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NCT03096366 · ClinicalTrials.gov registry record · NA

Does Blood Flow Restriction Training Improve Quadriceps Function After Arthroscopic Knee Surgery?

A NA study of ACL Reconstruction and Quadriceps Atrophy, sponsored by The University of Texas Health Science Center, Houston.

Recruiting
Registry status
NA
Development phase
150
Enrollment target
1
Study location

NCT03096366: Recruiting NA study of ACL Reconstruction and Quadriceps Atrophy, sponsored by The University of Texas Health Science Center, Houston.

NCT03096366 is a NA study of ACL Reconstruction and Quadriceps Atrophy that is actively recruiting participants, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 150 participants, above the 96-participant average among 4 other ACL Reconstruction trials with a reported enrollment target (56% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03096366, a NA study of ACL Reconstruction and Quadriceps Atrophy, is actively recruiting participants, sponsored by The University of Texas Health Science Center, Houston.

RECRUITING
Registry status
NA
Development phase
150 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to evaluate the effectiveness of physical therapy (PT) plus BFR training compared to PT alone (without BFR training) after ACL reconstruction in patients who require extended limited weight bearing through assessment of patient reported outcomes and functional testing. The hypothesis is that PT plus BFR training will mitigate the loss of quadriceps muscle cross-sectional area, strength, and function while also improving early clinical and functional results.

Primary Outcome

Initiation of PT is 1 month after surgery

Interventions

  • DEVICE Blood flow restriction
  • OTHER Physical therapy

Study Locations (1)

Texas

  • The University of Texas Health Science Center at Houston - Houston

Trial Details

FieldValue
Enrollment Target 150 participants
Start Date 2017-11-21
Est. Completion 2022-12
Phase NA

What NCT03096366 shows while recruiting

NCT03096366 is an interventional study that assigns participants to a tested intervention. The registered 150 participants enrollment target is mid-sized for trials with a published cap, above the 96-participant average among 4 other ACL Reconstruction trials with a reported enrollment target (56% higher).

The record links to 2 conditions, with ACL Reconstruction appearing as the primary indexed condition, and to 2 interventions - of which Blood flow restriction is the first listed.

NCT03096366 reports a single indexed study location in Texas.

Frequently Asked Questions

What is clinical trial NCT03096366 about?

NCT03096366 is a clinical study titled "Does Blood Flow Restriction Training Improve Quadriceps Function After Arthroscopic Knee Surgery?". The purpose of this study is to evaluate the effectiveness of physical therapy (PT) plus BFR training compared to PT alone (without BFR training) after ACL reconstruction in patients who require extended limited weight bearing through assessment of patient reported outcomes and functional testing. T...

What is the current status of trial NCT03096366?

This trial is currently recruiting. It is a NA study. The enrollment target is 150 participants. The study started on 2017-11-21. Estimated completion is 2022-12.

What conditions does trial NCT03096366 study?

This clinical trial studies the following conditions: ACL Reconstruction, Quadriceps Atrophy.

What interventions are being tested in trial NCT03096366?

The interventions under investigation include: Blood flow restriction (DEVICE), Physical therapy (OTHER).

Who is sponsoring clinical trial NCT03096366?

This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03096366 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT03096366, the US trial registry maintained by the National Library of Medicine. NCT03096366 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.