Trial Outcomes & Findings for A Real World Evaluation of the ELUVIA Stent in Subjects With Lesions Located in the Femoropopliteal Arteries (NCT NCT03037411)
NCT ID: NCT03037411
Last Updated: 2026-03-31
Results Overview
The EQ-5D assesses five dimensions (mobility, self-care, usual activities, pain/discomfort, anxiety/depression) of health-related quality of life responses assigned by the participants. The values are anchored at 1 (best) to 0 (worst). The vales for the visual analog score takes values from 100 (best) to 0 (worst). The index value is comparable across the baseline, 12- and 24-Months timepoints.
COMPLETED
291 participants
Baseline,12 and 24 months
2026-03-31
Participant Flow
291 participants were enrolled and implanted with the Eluvia Stent
Participant milestones
| Measure |
ELUVIA Drug-Eluting Vascular Stent System
Peripheral stenting of superficial Femoral Artery (SFA) and/or Proximal Popliteal Artery (PPA) lesions
|
|---|---|
|
Overall Study
STARTED
|
291
|
|
Overall Study
COMPLETED
|
216
|
|
Overall Study
NOT COMPLETED
|
75
|
Reasons for withdrawal
| Measure |
ELUVIA Drug-Eluting Vascular Stent System
Peripheral stenting of superficial Femoral Artery (SFA) and/or Proximal Popliteal Artery (PPA) lesions
|
|---|---|
|
Overall Study
Withdrawal by Subject
|
7
|
|
Overall Study
Adverse Event
|
1
|
|
Overall Study
Physician Decision
|
1
|
|
Overall Study
Lost to Follow-up
|
18
|
|
Overall Study
Visit Missed
|
19
|
|
Overall Study
Death
|
28
|
|
Overall Study
Site indicated follow up was not possible
|
1
|
Baseline Characteristics
Not all subjects had this comorbidity
Baseline characteristics by cohort
| Measure |
ELUVIA Drug-Eluting Vascular Stent System
n=291 Participants
Peripheral stenting of superficial Femoral Artery (SFA) and/or Proximal Popliteal Artery (PPA) lesions
|
|---|---|
|
Race/Ethnicity, Customized
American Indian or Alaskan native
|
1 Participants
n=291 Participants
|
|
Age, Continuous
|
69.7 years
STANDARD_DEVIATION 9.6 • n=291 Participants
|
|
Sex: Female, Male
Female
|
50 Participants
n=291 Participants
|
|
Sex: Female, Male
Male
|
241 Participants
n=291 Participants
|
|
Race/Ethnicity, Customized
Asian
|
0 Participants
n=291 Participants
|
|
Race/Ethnicity, Customized
Black of African heritage
|
0 Participants
n=291 Participants
|
|
Race/Ethnicity, Customized
Caucasian
|
275 Participants
n=291 Participants
|
|
Race/Ethnicity, Customized
Hispanic or Latino
|
7 Participants
n=291 Participants
|
|
Race/Ethnicity, Customized
Native Hawaiian or other Pacific Islander
|
0 Participants
n=291 Participants
|
|
Race/Ethnicity, Customized
Other
|
0 Participants
n=291 Participants
|
|
Race/Ethnicity, Customized
Not disclosed
|
8 Participants
n=291 Participants
|
|
Region of Enrollment
Belgium
|
94 participants
n=291 Participants
|
|
Region of Enrollment
Italy
|
90 participants
n=291 Participants
|
|
Region of Enrollment
France
|
14 participants
n=291 Participants
|
|
Region of Enrollment
Spain
|
93 participants
n=291 Participants
|
|
Smoking Status
Current
|
98 Participants
n=291 Participants
|
|
Smoking Status
Never
|
38 Participants
n=291 Participants
|
|
Smoking Status
Previous
|
139 Participants
n=291 Participants
|
|
Smoking Status
Unknown
|
16 Participants
n=291 Participants
|
|
Current Diabetes Mellitus
|
141 Participants
n=291 Participants
|
|
History of Hyperlipidemia requiring medication
|
197 Participants
n=291 Participants
|
|
History of Hypertension requiring medication
|
229 Participants
n=291 Participants
|
|
History of Chronic Obstructive Pulmonary Disease
|
45 Participants
n=291 Participants
|
|
Cardiac history
Historic of coronary artery disease
|
90 Participants
n=291 Participants
|
|
Cardiac history
History of Myocardial infarction (MI)
|
61 Participants
n=291 Participants
|
|
Cardiac history
History of congestive heart failure
|
22 Participants
n=291 Participants
|
|
New York Heat Assoc. (NHYA) Classification
Class I
|
4 Participants
n=22 Participants • Not all subjects had this comorbidity
|
|
New York Heat Assoc. (NHYA) Classification
Class II
|
7 Participants
n=22 Participants • Not all subjects had this comorbidity
|
|
New York Heat Assoc. (NHYA) Classification
Class III
|
0 Participants
n=22 Participants • Not all subjects had this comorbidity
|
|
New York Heat Assoc. (NHYA) Classification
Class IV
|
2 Participants
n=22 Participants • Not all subjects had this comorbidity
|
|
New York Heat Assoc. (NHYA) Classification
Unknown
|
9 Participants
n=22 Participants • Not all subjects had this comorbidity
|
|
Current Anginal Status
None
|
265 Participants
n=291 Participants
|
|
Current Anginal Status
Stable angina
|
6 Participants
n=291 Participants
|
|
Current Anginal Status
Unstable angina
|
3 Participants
n=291 Participants
|
|
Current Anginal Status
Unknown
|
17 Participants
n=291 Participants
|
|
History of Renal Insufficiency
|
44 Participants
n=291 Participants
|
|
History of Peripheral Vascular Disease
|
57 Participants
n=291 Participants
|
|
History of Endovascular Interventions in Target Vessel
|
43 Participants
n=291 Participants
|
|
Target Lesion Length
|
98.4 mm
STANDARD_DEVIATION 73.6 • n=291 Participants
|
|
Chronic Total Occlusion
|
145 Participants
n=291 Participants
|
PRIMARY outcome
Timeframe: Baseline,12 and 24 monthsPopulation: The number analyzed for each row is based on the number of participants that completed the assessment during the specified visit.
The EQ-5D assesses five dimensions (mobility, self-care, usual activities, pain/discomfort, anxiety/depression) of health-related quality of life responses assigned by the participants. The values are anchored at 1 (best) to 0 (worst). The vales for the visual analog score takes values from 100 (best) to 0 (worst). The index value is comparable across the baseline, 12- and 24-Months timepoints.
Outcome measures
| Measure |
ELUVIA Drug-Eluting Vascular Stent System
n=291 Participants
Peripheral stenting of superficial Femoral Artery (SFA) and/or Proximal Popliteal Artery (PPA) lesions
|
|---|---|
|
Participant Quality-of-Life Changes Via EuroQol 5 Dimension (EQ-5D) Questionnaire.
Baseline Index Value
|
0.7 score on a scale
Standard Deviation 0.2
|
|
Participant Quality-of-Life Changes Via EuroQol 5 Dimension (EQ-5D) Questionnaire.
12-month Index Value
|
0.9 score on a scale
Standard Deviation .02
|
|
Participant Quality-of-Life Changes Via EuroQol 5 Dimension (EQ-5D) Questionnaire.
24-month Index Value
|
0.8 score on a scale
Standard Deviation 0.2
|
|
Participant Quality-of-Life Changes Via EuroQol 5 Dimension (EQ-5D) Questionnaire.
Baseline - Visual Analogue Scale
|
60.9 score on a scale
Standard Deviation 18.8
|
|
Participant Quality-of-Life Changes Via EuroQol 5 Dimension (EQ-5D) Questionnaire.
12-month - Visual Analogue Scale
|
73.4 score on a scale
Standard Deviation 16.8
|
|
Participant Quality-of-Life Changes Via EuroQol 5 Dimension (EQ-5D) Questionnaire.
24-month - Visual Analogue Scale
|
72.0 score on a scale
Standard Deviation 17.2
|
SECONDARY outcome
Timeframe: 12 and 24 monthsPopulation: The number analyzed for each row is based on the number of participants that completed the assessment during the specified visit.
Improvement was calculated by comparing the scores from 12- and 24-Months to the baseline scores and presenting the number of participants that showed improvement at 12- and 24-Months. The WIQ measures the improvement as reported by participants in their walking distance, walking speed, stair-climbing ability and improvement in their PAD symptoms pre-procedure (baseline) compared to 12 months and compared to 24 months. The improvement at those time points is measured as percent improvement.
Outcome measures
| Measure |
ELUVIA Drug-Eluting Vascular Stent System
n=291 Participants
Peripheral stenting of superficial Femoral Artery (SFA) and/or Proximal Popliteal Artery (PPA) lesions
|
|---|---|
|
Number of Participants With Improvement on the Walking Impairment Questionnaire
12 Month - Distance Score - Number of Participants Improved
|
166 Participants
|
|
Number of Participants With Improvement on the Walking Impairment Questionnaire
24 Month - Distance Score - Number of Participants Improved
|
156 Participants
|
|
Number of Participants With Improvement on the Walking Impairment Questionnaire
12 Month - Speed Score - Number of Participants Improved
|
158 Participants
|
|
Number of Participants With Improvement on the Walking Impairment Questionnaire
24 Month - Speed Score - Number of Participants Improved
|
140 Participants
|
|
Number of Participants With Improvement on the Walking Impairment Questionnaire
12 Month - Stair Climbing Score - Number of Participants Improved
|
132 Participants
|
|
Number of Participants With Improvement on the Walking Impairment Questionnaire
24 Month - Stair Climbing Score - Number of Participants Improved
|
116 Participants
|
|
Number of Participants With Improvement on the Walking Impairment Questionnaire
12 Month - Peripheral Arterial Disease Specific Question Score - Number of Participants Improved
|
170 Participants
|
|
Number of Participants With Improvement on the Walking Impairment Questionnaire
24 Month - Peripheral Arterial Disease Specific Question Score - Number of Participants Improved
|
153 Participants
|
SECONDARY outcome
Timeframe: 12 and 24 monthsPopulation: The number analyzed for each row is based on the number of participants that completed the assessment during the specified visit.
The Rutherford Classification describes the different stages of peripheral artery disease (PAD) from a score of 0 (no PAD) to 6 (critical limb ischemia with major tissue loss). The percentages represent the percent of participants that had sustained clinical improvement from baseline to 12 months and baseline to 24 months. Sustained clinical improvement means their Rutherford Class improved by one or more categories compared with baseline. Number of participants with improved Rutherford Classification at 12- and 24-Months when compared to baseline. Primary Sustained Clinical Improvement is improvement in Rutherford Classification of one or more categories as compared to baseline without the need for repeat target lesion revascularization (TLR). Secondary Sustained Clinical Improvement is improvement in Rutherford classification of one or more categories as compared to baseline including those participants with repeat TLR.
Outcome measures
| Measure |
ELUVIA Drug-Eluting Vascular Stent System
n=291 Participants
Peripheral stenting of superficial Femoral Artery (SFA) and/or Proximal Popliteal Artery (PPA) lesions
|
|---|---|
|
Number of Participants With Improved Rutherford Classification Indicating Rate of Primary and Secondary Sustained Clinical Improvement
12 Month - Primary Sustained Clinical Improvement
|
187 Participants
|
|
Number of Participants With Improved Rutherford Classification Indicating Rate of Primary and Secondary Sustained Clinical Improvement
24 Month - Primary Sustained Clinical Improvement
|
165 Participants
|
|
Number of Participants With Improved Rutherford Classification Indicating Rate of Primary and Secondary Sustained Clinical Improvement
12 Month - Secondary Sustained Clinical Improvement
|
203 Participants
|
|
Number of Participants With Improved Rutherford Classification Indicating Rate of Primary and Secondary Sustained Clinical Improvement
24 Month - Secondary Sustained Clinical Improvement
|
185 Participants
|
SECONDARY outcome
Timeframe: 12 and 24 monthsPopulation: The number analyzed for each row is based on the number of participants that completed the assessment during the specified visit.
Number of participants with improvement in Ankle-Brachial Index (ABI) at 12- and 24-Months compared to baseline. Hemodynamic Improvement is defined as an increase in ABI of \>= 0.10 or to an ABI \>= 0.90 as compared to baseline without the need for repeat TLR. The ABI measures the arterial pressure in the leg compared to the arterial pressure in the arm. The higher the value, the better the blood flow. Improvement is defined as an increase in the ABI by greater than or equal to 0.10 compared with baseline or to an ABI greater than or equal to 0.90. The percentages in the table represent the patients that demonstrated an improvement in their ABI from baseline to 12 months and baseline to 24-months.
Outcome measures
| Measure |
ELUVIA Drug-Eluting Vascular Stent System
n=291 Participants
Peripheral stenting of superficial Femoral Artery (SFA) and/or Proximal Popliteal Artery (PPA) lesions
|
|---|---|
|
Number of Participants With Hemodynamic Improvement
12 Month - Hemodynamic Improvement
|
137 Participants
|
|
Number of Participants With Hemodynamic Improvement
24 Month - Hemodynamic Improvement
|
102 Participants
|
|
Number of Participants With Hemodynamic Improvement
12 Month - Hemodynamic Improvement (Including TLR)
|
146 Participants
|
|
Number of Participants With Hemodynamic Improvement
24 Month - Hemodynamic Improvement (Including TLR)
|
114 Participants
|
SECONDARY outcome
Timeframe: 1, 6, 12 and 24 monthsChanges in healthcare utilization over time
Outcome measures
Outcome data not reported
OTHER_PRE_SPECIFIED outcome
Timeframe: During stenting procedureNumber of participants that successfully received Eluvia stent. Technical success defined as implanted and achieving residual angiographic stenosis no greater than 30% assessed visually.
Outcome measures
| Measure |
ELUVIA Drug-Eluting Vascular Stent System
n=291 Participants
Peripheral stenting of superficial Femoral Artery (SFA) and/or Proximal Popliteal Artery (PPA) lesions
|
|---|---|
|
Number of Participants With Technical Success of the Stenting Procedure
|
288 Participants
|
OTHER_PRE_SPECIFIED outcome
Timeframe: within 24 hours of stenting procedureNumber of participants with successful procedures. Procedural success defined as technical success with no major adverse events (MAEs) noted within 24 hours of the stenting procedure.
Outcome measures
| Measure |
ELUVIA Drug-Eluting Vascular Stent System
n=291 Participants
Peripheral stenting of superficial Femoral Artery (SFA) and/or Proximal Popliteal Artery (PPA) lesions
|
|---|---|
|
Number of Participants With Procedural Success of the Stenting Procedure
|
288 Participants
|
OTHER_PRE_SPECIFIED outcome
Timeframe: 12 and 24 monthsPopulation: Denominators for the cumulative rate is based on 1) participants with events, and 2) participants with no events but their follow-up time reach on (or beyond) the earliest visit window.
Number of participants with Clinical Events Committee (CEC) adjudicated MAEs at 12- and 24-Months cumulatively. The MAEs are defined as all causes of death, target limb major amputation and/or Target Lesion Revascularization rate. A participant can be present in more than one sub-category.
Outcome measures
| Measure |
ELUVIA Drug-Eluting Vascular Stent System
n=291 Participants
Peripheral stenting of superficial Femoral Artery (SFA) and/or Proximal Popliteal Artery (PPA) lesions
|
|---|---|
|
Number of Participants With a Major Adverse Event (MAE)
12 Month - All Deaths
|
23 Participants
|
|
Number of Participants With a Major Adverse Event (MAE)
12 Month - Major Amputation
|
6 Participants
|
|
Number of Participants With a Major Adverse Event (MAE)
12 Month - Target Lesion Revascularization
|
25 Participants
|
|
Number of Participants With a Major Adverse Event (MAE)
24 Month - All Deaths
|
28 Participants
|
|
Number of Participants With a Major Adverse Event (MAE)
24 Month - Major Amputation
|
6 Participants
|
|
Number of Participants With a Major Adverse Event (MAE)
24 Month - Target Lesion Revascularization
|
30 Participants
|
OTHER_PRE_SPECIFIED outcome
Timeframe: 12 and 24 monthsPopulation: Analysis utilized a Kaplan-Meier for calculation. The count of participants is estimated from the number of participants and the primary patency rate at 12 Months and 24 Months.
The numbers represent the percentage of patients that were event free at 12 and 24 months (i.e. didn't have a TLR).
Outcome measures
| Measure |
ELUVIA Drug-Eluting Vascular Stent System
n=291 Participants
Peripheral stenting of superficial Femoral Artery (SFA) and/or Proximal Popliteal Artery (PPA) lesions
|
|---|---|
|
Percentage of Participants With Primary Patency at 12- and 24-Months Post Procedure
12 Month - Primary Patency
|
268 Participants
|
|
Percentage of Participants With Primary Patency at 12- and 24-Months Post Procedure
24 Month - Primary Patency
|
251 Participants
|
OTHER_PRE_SPECIFIED outcome
Timeframe: 12 and 24 monthsPopulation: Denominators for the cumulative rate will be based on 1) participants with events, and 2) participants with no events but their follow-up time reach on (or beyond) the earliest visit window.
The cumulative number of participants that received a clinically-driven target lesion revascularization after the stenting procedure.
Outcome measures
| Measure |
ELUVIA Drug-Eluting Vascular Stent System
n=291 Participants
Peripheral stenting of superficial Femoral Artery (SFA) and/or Proximal Popliteal Artery (PPA) lesions
|
|---|---|
|
Number of Participants With a Clinically-driven Target Lesion Revascularization (TLR)
12 Month - Clinical Driven TLR
|
24 Participants
|
|
Number of Participants With a Clinically-driven Target Lesion Revascularization (TLR)
24 Month - Clinical Driven TLR
|
29 Participants
|
OTHER_PRE_SPECIFIED outcome
Timeframe: 12 and 24 monthsPopulation: Denominators for the cumulative rate will be based on 1) participants with events, and 2) participants with no events but their follow-up time reach on (or beyond) the earliest visit window.
The cumulative number of participants that received a clinically-driven target vessel revascularization after the stenting procedure.
Outcome measures
| Measure |
ELUVIA Drug-Eluting Vascular Stent System
n=291 Participants
Peripheral stenting of superficial Femoral Artery (SFA) and/or Proximal Popliteal Artery (PPA) lesions
|
|---|---|
|
Number of Participants With a Clinically-driven Target Vessel Revascularization (TVR)
12 Month - Clinically Driven TVR
|
29 Participants
|
|
Number of Participants With a Clinically-driven Target Vessel Revascularization (TVR)
24 Month - Clinically Driven TVR
|
35 Participants
|
OTHER_PRE_SPECIFIED outcome
Timeframe: Baseline, 12 and 24 monthsPopulation: The number analyzed for each timepoint is based on the number of participants that completed the assessment during the specified visit.
Rutherford Classification: 0\. Asymptomatic - Normal Treadmill /stress test 1. Mild claudication - Completes treadmill exercise; ankle pressure (AP) after exercise \<50mm Hg, but \>25 mm Hg less than blood pressure (BP) 2. Moderate claudication - Between categories 1 and 3 3. Severe claudication - Cannot complete treadmill exercise and AP after exercise \<50 mm Hg 4. Ischemic rest pain - Resting AP \<40 mm Hg, flat or barely pulsatile ankle or metatarsal pulse volume recording (PVR); toe pressure (TP) \<30 mm Hg 5. Minor tissue loss-nonhealing ulcer, focal gangrene with diffuse pedal edema - Resting AP \<60 mm Hg, ankle or metatarsal (MT) PVR flat or barely pulsatile; TP \<40 mm Hg 6. Major tissue loss-extending above MT level - Same as Category 5
Outcome measures
| Measure |
ELUVIA Drug-Eluting Vascular Stent System
n=291 Participants
Peripheral stenting of superficial Femoral Artery (SFA) and/or Proximal Popliteal Artery (PPA) lesions
|
|---|---|
|
Participant Distribution on the Rutherford Classification at Baseline, 12-, and 24- Month
Baseline - Category 0: Asymptomatic
|
2 Participants
|
|
Participant Distribution on the Rutherford Classification at Baseline, 12-, and 24- Month
Baseline - Category 1: Mild claudication
|
2 Participants
|
|
Participant Distribution on the Rutherford Classification at Baseline, 12-, and 24- Month
Baseline - Category 2: Moderate claudication
|
70 Participants
|
|
Participant Distribution on the Rutherford Classification at Baseline, 12-, and 24- Month
Baseline - Category 3: Severe claudication
|
108 Participants
|
|
Participant Distribution on the Rutherford Classification at Baseline, 12-, and 24- Month
Baseline - Category 4: Ischemic rest pain
|
27 Participants
|
|
Participant Distribution on the Rutherford Classification at Baseline, 12-, and 24- Month
Baseline - Category 5: Minor tissue loss
|
71 Participants
|
|
Participant Distribution on the Rutherford Classification at Baseline, 12-, and 24- Month
Baseline - Category 6: Major tissue loss
|
10 Participants
|
|
Participant Distribution on the Rutherford Classification at Baseline, 12-, and 24- Month
12 Month - Category 0: Asymptomatic
|
149 Participants
|
|
Participant Distribution on the Rutherford Classification at Baseline, 12-, and 24- Month
12 Month - Category 1: Mild claudication
|
33 Participants
|
|
Participant Distribution on the Rutherford Classification at Baseline, 12-, and 24- Month
12 Month - Category 2: Moderate claudication
|
27 Participants
|
|
Participant Distribution on the Rutherford Classification at Baseline, 12-, and 24- Month
12 Month - Category 3: Severe claudication
|
5 Participants
|
|
Participant Distribution on the Rutherford Classification at Baseline, 12-, and 24- Month
12 Month - Category 4: Ischemic rest pain
|
2 Participants
|
|
Participant Distribution on the Rutherford Classification at Baseline, 12-, and 24- Month
12 Month - Category 5: Minor tissue loss
|
6 Participants
|
|
Participant Distribution on the Rutherford Classification at Baseline, 12-, and 24- Month
12 Month - Category 6: Major tissue loss
|
3 Participants
|
|
Participant Distribution on the Rutherford Classification at Baseline, 12-, and 24- Month
24 Month - Category 0: Asymptomatic
|
139 Participants
|
|
Participant Distribution on the Rutherford Classification at Baseline, 12-, and 24- Month
24 Month - Category 1: Mild claudication
|
30 Participants
|
|
Participant Distribution on the Rutherford Classification at Baseline, 12-, and 24- Month
24 Month - Category 2: Moderate claudication
|
19 Participants
|
|
Participant Distribution on the Rutherford Classification at Baseline, 12-, and 24- Month
24 Month - Category 3: Severe claudication
|
9 Participants
|
|
Participant Distribution on the Rutherford Classification at Baseline, 12-, and 24- Month
24 Month - Category 4: Ischemic rest pain
|
1 Participants
|
|
Participant Distribution on the Rutherford Classification at Baseline, 12-, and 24- Month
24 Month - Category 5: Minor tissue loss
|
4 Participants
|
|
Participant Distribution on the Rutherford Classification at Baseline, 12-, and 24- Month
24 Month - Category 6: Major tissue loss
|
1 Participants
|
Adverse Events
ELUVIA Drug-Eluting Vascular Stent System
Serious adverse events
| Measure |
ELUVIA Drug-Eluting Vascular Stent System
n=291 participants at risk
Peripheral stenting of superficial Femoral Artery (SFA) and/or Proximal Popliteal Artery (PPA) lesions
|
|---|---|
|
Vascular disorders
Gangrene
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Infections and infestations
Bacteriemia
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Cardiac disorders
Cardiac Failure
|
0.69%
2/291 • Number of events 2 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Nervous system disorders
Cerebrovascular Accident
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
General disorders
Death (Unknown)
|
2.1%
6/291 • Number of events 6 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Infections and infestations
Abdominal Sepsis
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Gastrointestinal disorders
Intestinal Ischemia
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Vascular disorders
Extremity Necrosis
|
2.1%
6/291 • Number of events 6 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Infections and infestations
Osteomyelitis
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Injury, poisoning and procedural complications
Post Procedural Complication
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Vascular disorders
Peripheral Arterial Occlusive Disease
|
1.0%
3/291 • Number of events 4 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Vascular disorders
Peripheral Artery Occlusion
|
1.7%
5/291 • Number of events 7 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Vascular disorders
Artery Dissection
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Vascular disorders
Peripheral Artery Stenosis
|
2.7%
8/291 • Number of events 8 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Vascular disorders
Peripheral Ischemia
|
1.0%
3/291 • Number of events 3 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Infections and infestations
Pneumonia
|
1.0%
3/291 • Number of events 3 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Rectal Cancer
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Respiratory, thoracic and mediastinal disorders
Respiratory Failure
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Respiratory, thoracic and mediastinal disorders
Respiratory Insufficiency
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Infections and infestations
Sepsis
|
0.69%
2/291 • Number of events 2 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
General disorders
Vascular Stent Thrombosis
|
3.4%
10/291 • Number of events 14 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
General disorders
Vascular Stent Occlusion
|
2.7%
8/291 • Number of events 8 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
General disorders
Vascular Stent Stenosis
|
2.7%
8/291 • Number of events 8 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Infections and infestations
Wound Infection
|
0.34%
1/291 • Number of events 2 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Infections and infestations
COVID-19 Pneumonia
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
General disorders
Stent Stenosis
|
0.69%
2/291 • Number of events 2 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
General disorders
Stent Restenosis
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Vascular disorders
Vascular Pseudoaneurysm
|
2.4%
7/291 • Number of events 7 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Vascular disorders
Vascular Disorders
|
1.4%
4/291 • Number of events 4 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Vascular disorders
Arterial Disorder
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Vascular disorders
Arterial Restenosis
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Vascular disorders
Dry Gangrene
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Vascular disorders
Peripheral Artery Restenosis
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Surgical and medical procedures
Toe Amputation
|
1.7%
5/291 • Number of events 6 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Surgical and medical procedures
Foot Amputation
|
0.69%
2/291 • Number of events 2 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Surgical and medical procedures
Leg Amputation
|
0.69%
2/291 • Number of events 2 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Surgical and medical procedures
Finger Amputation
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Surgical and medical procedures
Limb Amputation
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Infections and infestations
Diabetic Foot Infection
|
0.69%
2/291 • Number of events 2 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Infections and infestations
Septic Shock
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Cardiac disorders
Myocardial Infarction
|
0.69%
2/291 • Number of events 2 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Cardiac disorders
Arrhythmia
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Cardiac disorders
Cardiopulmonary failure
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Renal Neoplasm
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Investigations
Blood creatinine increased
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Respiratory, thoracic and mediastinal disorders
Dyspnoea
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Skin and subcutaneous tissue disorders
Wound
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Surgical and medical procedures
Arterial Puncture
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
Other adverse events
| Measure |
ELUVIA Drug-Eluting Vascular Stent System
n=291 participants at risk
Peripheral stenting of superficial Femoral Artery (SFA) and/or Proximal Popliteal Artery (PPA) lesions
|
|---|---|
|
Vascular disorders
Haematoma
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Vascular disorders
Extremity Necrosis
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Vascular disorders
Artery Dissection
|
1.0%
3/291 • Number of events 3 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
General disorders
Vascular Stent Stenosis
|
2.1%
6/291 • Number of events 6 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Surgical and medical procedures
Toe Amputation
|
1.0%
3/291 • Number of events 3 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
Vascular disorders
Vascular Pseudoaneurysm
|
0.34%
1/291 • Number of events 1 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
General disorders
Vascular Stent Occlusion
|
1.0%
3/291 • Number of events 3 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
|
General disorders
Vascular Stent Thrombosis
|
1.4%
4/291 • Number of events 4 • Major Adverse Events (all cause death, major amputation, and TLR) were collected through 24-months of follow-up.
|
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place
Restriction type: OTHER