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NCT02746458 · ClinicalTrials.gov registry record · NA
Rehabilitation Enhanced by Partial Arterial Inflow Restrictions
A NA study of Closed Femur Fracture, sponsored by Major Extremity Trauma Research Consortium.
- Active
- Registry status
- NA
- Development phase
- 250
- Enrollment target
- 8
- Study locations
NCT02746458 is a NA study of Closed Femur Fracture that is active but no longer recruiting, run by Major Extremity Trauma Research Consortium. The registered enrollment target is 250 participants. The trial reports 8 study locations across 6 states.
The verdict
NCT02746458, a NA study of Closed Femur Fracture, is active but no longer recruiting, sponsored by Major Extremity Trauma Research Consortium.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 250 participants
- Enrollment target
- 8
- Study locations
Study Summary
The Rehabilitation Enhanced by Partial Arterial Inflow Restriction (REPAIR) Study will be conducted in a patient population of individuals recovering from a traumatic diaphyseal fracture of the femur. Although the intervention can be used for any patient with muscle weakness following trauma, the persistent thigh weakness that follows a femur fracture provides a perfect model for evaluating the effectiveness of the REPAIR protocol.
Conditions Studied
Interventions
- OTHER Blood Flow Restriction
- DEVICE Delfi PTSII Tourniquet System
Study Locations (8)
Maryland
- University of Maryland Medical Center - Baltimore
- Walter Reed National Military Medical Center - Bethesda
Texas
- University of Texas Health Science Center at Houston - Houston
- San Antonio Military Medical Center - San Antonio
Indiana
- Methodist Hospital - Indianapolis
Missouri
- Barnes Jewish Hospital - St Louis
North Carolina
- Carolinas Medical Center - Charlotte
Ohio
- MetroHealth - Cleveland
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 250 participants |
| Start Date | 2016-04-01 |
| Est. Completion | 2024-08-01 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02746458
The ClinicalTrials.gov registry entry for NCT02746458 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 250 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Major Extremity Trauma Research Consortium, which has 30 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Closed Femur Fracture appearing as the primary indexed condition, and to 2 interventions - of which Blood Flow Restriction is the first listed.
NCT02746458 reports 8 study locations spanning 6 distinct geographic areas - top geographies include Maryland, Texas, Indiana.
Frequently Asked Questions
What is clinical trial NCT02746458 about?
NCT02746458 is a clinical study titled "Rehabilitation Enhanced by Partial Arterial Inflow Restrictions". The Rehabilitation Enhanced by Partial Arterial Inflow Restriction (REPAIR) Study will be conducted in a patient population of individuals recovering from a traumatic diaphyseal fracture of the femur. Although the intervention can be used for any patient with muscle weakness following trauma, the pe...
What is the current status of trial NCT02746458?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 250 participants. The study started on 2016-04-01. Estimated completion is 2024-08-01.
What conditions does trial NCT02746458 study?
This clinical trial studies the following conditions: Closed Femur Fracture.
What interventions are being tested in trial NCT02746458?
The interventions under investigation include: Blood Flow Restriction (OTHER), Delfi PTSII Tourniquet System (DEVICE).
Who is sponsoring clinical trial NCT02746458?
This trial is sponsored by Major Extremity Trauma Research Consortium, which has 30 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02746458 being conducted?
This trial has 8 study locations across Indiana, Maryland, Missouri, North Carolina, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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