Trial Outcomes & Findings for Effect of Emergency Department Bedside Compression Ultrasonography on Door-to-Disposition Time in Patients Suspicious for Lower Extremity Deep Venous Thrombosis (NCT NCT05682040)

NCT ID: NCT05682040

Last Updated: 2026-07-30

Results Overview

Completion time in minutes for point of care ultrasound (POCUS) in the emergency department followed by formal lower extremity (LE) doppler in radiology department prior to patient disposition from emergency department.

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

65 participants

Primary outcome timeframe

Emergency Department admission to Disposition from Emergency Department

Results posted on

2026-07-30

Participant Flow

Participant milestones

Participant milestones
Measure
Active
Point of Care Ultrasound (Bedside Compression Ultrasonography) in Emergency Department followed by Formal Lower Extremity Doppler in Radiology
Overall Study
STARTED
65
Overall Study
COMPLETED
56
Overall Study
NOT COMPLETED
9

Reasons for withdrawal

Reasons for withdrawal
Measure
Active
Point of Care Ultrasound (Bedside Compression Ultrasonography) in Emergency Department followed by Formal Lower Extremity Doppler in Radiology
Overall Study
excluded
9

Baseline Characteristics

Race and Ethnicity were not collected from any participant.

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Active
n=56 Participants
Point of Care Ultrasound (Bedside Compression Ultrasonography) in Emergency Department followed by Formal Lower Extremity Doppler in Radiology
Age, Continuous
59 years
n=56 Participants
Sex: Female, Male
Female
34 Participants
n=56 Participants
Sex: Female, Male
Male
22 Participants
n=56 Participants
Region of Enrollment
United States
56 Participants
n=56 Participants

PRIMARY outcome

Timeframe: Emergency Department admission to Disposition from Emergency Department

Completion time in minutes for point of care ultrasound (POCUS) in the emergency department followed by formal lower extremity (LE) doppler in radiology department prior to patient disposition from emergency department.

Outcome measures

Outcome measures
Measure
Active
n=56 Participants
The time in minutes for completion of Point of Care Ultrasound (Bedside Compression Ultrasonography) followed by time in minutes of Formal Lower Extremity Doppler until disposition from Emergency Department.
Time to Completion of Point of Care Ultrasound in Emergency Room and Lower Extremity Doppler Prior to Disposition
Completion Bedside US
7 minutes
Interval 2.0 to 20.0
Time to Completion of Point of Care Ultrasound in Emergency Room and Lower Extremity Doppler Prior to Disposition
Completion formal US
41 minutes
Interval 16.0 to 255.0
Time to Completion of Point of Care Ultrasound in Emergency Room and Lower Extremity Doppler Prior to Disposition
Disposition
241 minutes
Interval 50.0 to 385.0

SECONDARY outcome

Timeframe: Upon completion of POCUS and formal lower extremity doppler until disposition from Emergency Department

The accuracy of POCUS vs formal doppler in making the diagnosis of lower extremity deep vein thrombosis in the number of participants who completed the study.

Outcome measures

Outcome measures
Measure
Active
n=56 Participants
The time in minutes for completion of Point of Care Ultrasound (Bedside Compression Ultrasonography) followed by time in minutes of Formal Lower Extremity Doppler until disposition from Emergency Department.
Accuracy of POCUS vs Formal Lower Extremity Doppler
True Positive (beside & formal positive)
2 Participants
Accuracy of POCUS vs Formal Lower Extremity Doppler
False Positive (Bedside positive/ negative)
4 Participants
Accuracy of POCUS vs Formal Lower Extremity Doppler
False Negative (Bedside negative/Formal +)
4 Participants
Accuracy of POCUS vs Formal Lower Extremity Doppler
True Negative (Bedside negative/ Formal Negative)
46 Participants

Adverse Events

Completed

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

Dr. Christopher Nedzlek

HenryFordHS

Phone: 17342236996

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place