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NCT04436523 · ClinicalTrials.gov registry record · NA
Blood Flow Restriction After Meniscus Repair
A NA study, sponsored by University of California, San Francisco.
- Terminated
- Registry status
- NA
- Development phase
- 15
- Enrollment target
NCT04436523 is a NA study that was terminated before completion, run by University of California, San Francisco. The registered enrollment target is 15 participants.
The verdict
NCT04436523, a NA study, was terminated before completion, sponsored by University of California, San Francisco.
- TERMINATED
- Registry status
- NA
- Development phase
- 15 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate post-operative outcomes after meniscus surgery in participants undergoing blood flow restriction training as a rehabilitative adjunct compared to those with standard rehabilitation.
Interventions
- OTHER Standard rehabilitation
- DEVICE Blood flow restriction (Delfi Personalized Tourniquet System)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 15 participants |
| Start Date | 2020-10-20 |
| Est. Completion | 2023-06-08 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04436523
The ClinicalTrials.gov registry entry for NCT04436523 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 15 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of California, San Francisco, which has 1,713 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Standard rehabilitation is the first listed.
NCT04436523 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT04436523 about?
NCT04436523 is a clinical study titled "Blood Flow Restriction After Meniscus Repair". The purpose of this study is to evaluate post-operative outcomes after meniscus surgery in participants undergoing blood flow restriction training as a rehabilitative adjunct compared to those with standard rehabilitation.
What is the current status of trial NCT04436523?
This trial is currently terminated. It is a NA study. The enrollment target is 15 participants. The study started on 2020-10-20. Estimated completion is 2023-06-08.
What interventions are being tested in trial NCT04436523?
The interventions under investigation include: Standard rehabilitation (OTHER), Blood flow restriction (Delfi Personalized Tourniquet System) (DEVICE).
Who is sponsoring clinical trial NCT04436523?
This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.
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