Effect of Emergency Department Bedside Compression Ultrasonography on Door-to-Disposition Time in Patients Suspicious for Lower Extremity Deep Venous Thrombosis
Sponsor
Henry Ford Health System (Other)
Overall Status
Completed
CT.gov ID
NCT05682040
Collaborator
(none)
50
1
1
7
7.2
Study Details
Study Description
Brief Summary
Comparing the disposition time of point of care ultrasound (POCUS) versus formal lower extremity doppler in emergency department patients.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Study Design
Study Type:
Interventional
Actual Enrollment
:
50 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Effect of Emergency Department Bedside Compression Ultrasonography on Door-to-Disposition Time in Patients Suspicious for Lower Extremity Deep Venous Thrombosis
Actual Study Start Date
:
Nov 1, 2017
Actual Primary Completion Date
:
Mar 1, 2018
Actual Study Completion Date
:
Jun 1, 2018
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Other: Active
|
Diagnostic Test: Bedside Compression Ultrasonography
Point of Care Ultrasound (Bedside Compression Ultrasonography) vs formal lower extremity Doppler
|
Outcome Measures
Primary Outcome Measures
- Time to disposition [3 months]
We measured the time to disposition from the emergency department for point of care ultrasound (POCUS) vs formal lower extremity (LE) doppler in radiology department.
Secondary Outcome Measures
- Accuracy of POCUS vs formal LE doppler [3 months]
We examined the accuracy of POCUS vs formal doppler in making the diagnosis of lower extremity deep vein thrombosis.
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria: Emergency Department patients presenting for lower extremity swelling concerning Deep vein thrombosis.
-
Exclusion Criteria: n/a
-
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Henry Ford Wyandotte Hospital | Wyandotte | Michigan | United States | 48192 |
Sponsors and Collaborators
- Henry Ford Health System
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Christopher Nedzlek,
Staff physician emergency department,
Henry Ford Health System
ClinicalTrials.gov Identifier:
NCT05682040
Other Study ID Numbers:
- 11243
First Posted:
Jan 12, 2023
Last Update Posted:
Jan 12, 2023
Last Verified:
Jan 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
Yes
Additional relevant MeSH terms: