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NCT03650374 · ClinicalTrials.gov registry record · NA
Effects of Contralateral Strength Training on Postoperative Strength Deficits in the Immobilized Lower Extremity
A NA study of Meniscus; Detachment, Current Injury, sponsored by NYU Langone Health.
- Recruiting
- Registry status
- NA
- Development phase
- 50
- Enrollment target
- 1
- Study location
NCT03650374: Recruiting NA study of Meniscus; Detachment, Current Injury, sponsored by NYU Langone Health.
NCT03650374 is a NA study of Meniscus; Detachment, Current Injury that is actively recruiting participants, run by NYU Langone Health. 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). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03650374, a NA study of Meniscus; Detachment, Current Injury, is actively recruiting participants, sponsored by NYU Langone Health.
- RECRUITING
- Registry status
- NA
- Development phase
- 50 participants
- Enrollment target
- 1
- Study location
Study Summary
This is a prospective, randomized controlled trial that will enroll patients undergoing unilateral meniscal root repair or meniscus transplant. The objective of this study is to determine if immediate postoperative strength training of the contralateral (non-surgical) lower extremity reduces postoperative loss of strength in an immobilized lower extremity. After the completion of surgery, patients will be randomized to either the experimental treatment (Group 1) or control group (Group II)for postoperative rehabilitation.
Primary Outcome
A patient-reported outcome measurement instrument, developed to assess the patient's opinion about their knee and associated problems.
Conditions Studied
Interventions
- OTHER Standard of Care Rehabilitation
- OTHER Experimental Strength Training
Study Locations (1)
New York
- New York University School of Medicine - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2021-09-01 |
| Est. Completion | 2025-12-01 |
| Phase | NA |
What NCT03650374 shows while recruiting
NCT03650374 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 1 condition, with Meniscus; Detachment, Current Injury appearing as the primary indexed condition, and to 2 interventions - of which Standard of Care Rehabilitation is the first listed.
NCT03650374 reports a single indexed study location in New York.
Frequently Asked Questions
What is clinical trial NCT03650374 about?
NCT03650374 is a clinical study titled "Effects of Contralateral Strength Training on Postoperative Strength Deficits in the Immobilized Lower Extremity". This is a prospective, randomized controlled trial that will enroll patients undergoing unilateral meniscal root repair or meniscus transplant. The objective of this study is to determine if immediate postoperative strength training of the contralateral (non-surgical) lower extremity reduces postope...
What is the current status of trial NCT03650374?
This trial is currently recruiting. It is a NA study. The enrollment target is 50 participants. The study started on 2021-09-01. Estimated completion is 2025-12-01.
What conditions does trial NCT03650374 study?
This clinical trial studies the following conditions: Meniscus; Detachment, Current Injury.
What interventions are being tested in trial NCT03650374?
The interventions under investigation include: Standard of Care Rehabilitation (OTHER), Experimental Strength Training (OTHER).
Who is sponsoring clinical trial NCT03650374?
This trial is sponsored by NYU Langone Health, which has 1,164 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03650374 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03650374's enrollment target sits among peer trials
50 1280th 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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