Trial Outcomes & Findings for Compass Device CVC Trial (NCT NCT03056859)
NCT ID: NCT03056859
Last Updated: 2024-06-27
Results Overview
Operator satisfaction (0-10 scale; 0=totally dissatisfied, 10=totally satisfied)
Recruitment status
COMPLETED
Target enrollment
20 participants
Primary outcome timeframe
15 minutes
Results posted on
2024-06-27
Participant Flow
Participant milestones
| Measure |
Enrolled Patients
Procedure: Central venous catheter placement with extravascular blood pressure transducer
|
|---|---|
|
Overall Study
STARTED
|
20
|
|
Overall Study
COMPLETED
|
20
|
|
Overall Study
NOT COMPLETED
|
0
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Race and Ethnicity were not collected from any participant.
Baseline characteristics by cohort
| Measure |
Enrolled Patients
n=20 Participants
Procedure: Central venous catheter placement with extravascular blood pressure transducer
|
|---|---|
|
Age, Continuous
|
64 years
n=20 Participants
|
|
Sex: Female, Male
Female
|
10 Participants
n=20 Participants
|
|
Sex: Female, Male
Male
|
10 Participants
n=20 Participants
|
|
Region of Enrollment
United States
|
20 participants
n=20 Participants
|
|
Body Mass Index
|
39.6 kg/m^2
n=20 Participants
|
PRIMARY outcome
Timeframe: 15 minutesOperator satisfaction (0-10 scale; 0=totally dissatisfied, 10=totally satisfied)
Outcome measures
| Measure |
Enrolled Patients
n=20 Participants
Procedure: Central venous catheter placement with extravascular blood pressure transducer
|
|---|---|
|
Operator Satisfaction
|
8 score on a scale
Interval 5.0 to 10.0
|
SECONDARY outcome
Timeframe: 15 minutesIncidence of arterial puncture
Outcome measures
| Measure |
Enrolled Patients
n=20 Participants
Procedure: Central venous catheter placement with extravascular blood pressure transducer
|
|---|---|
|
Arterial Puncture Incidence
|
0 Participants
|
SECONDARY outcome
Timeframe: 15 minutesPopulation: There were no arterial punctures observed during the study.
If arterial puncture occurred, list catheterization implement being manipulated at the time
Outcome measures
Outcome data not reported
Adverse Events
Enrolled Patients
Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Research Officer
University of New Mexico Anesthesiology Department
Phone: 505-272-2610
Email: [email protected]
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place