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NCT05682040 · ClinicalTrials.gov registry record · NA
Effect of Emergency Department Bedside Compression Ultrasonography on Door-to-Disposition Time in Patients Suspicious for Lower Extremity Deep Venous Thrombosis
A NA study, sponsored by Henry Ford Health System.
- Completed
- Registry status
- NA
- Development phase
- 50
- Enrollment target
NCT05682040: Completed NA study, sponsored by Henry Ford Health System.
NCT05682040 is a NA study that has completed, run by Henry Ford Health System. The registered enrollment target is 50 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05682040, a NA study, has completed, sponsored by Henry Ford Health System.
- COMPLETED
- Registry status
- NA
- Development phase
- 50 participants
- Enrollment target
Study Summary
Comparing the disposition time of point of care ultrasound (POCUS) versus formal lower extremity doppler in emergency department patients.
Primary Outcome
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.
Interventions
- DIAGNOSTIC_TEST Bedside Compression Ultrasonography
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2017-11-01 |
| Est. Completion | 2018-06-01 |
| Phase | NA |
What the finished NCT05682040 record still lists
NCT05682040 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).
The record links to 0 conditions, and to 1 intervention - of which Bedside Compression Ultrasonography is the first listed.
NCT05682040 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT05682040 about?
NCT05682040 is a clinical study titled "Effect of Emergency Department Bedside Compression Ultrasonography on Door-to-Disposition Time in Patients Suspicious for Lower Extremity Deep Venous Thrombosis". Comparing the disposition time of point of care ultrasound (POCUS) versus formal lower extremity doppler in emergency department patients.
What is the current status of trial NCT05682040?
This trial is currently completed. It is a NA study. The enrollment target is 50 participants. The study started on 2017-11-01. Estimated completion is 2018-06-01.
What interventions are being tested in trial NCT05682040?
The interventions under investigation include: Bedside Compression Ultrasonography (DIAGNOSTIC_TEST).
Who is sponsoring clinical trial NCT05682040?
This trial is sponsored by Henry Ford Health System, which has 234 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT05682040's enrollment target sits among peer trials
50 1279th of 2000 higher than 622 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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