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NCT06542705 · ClinicalTrials.gov registry record · NA
Effect of Internal Brace on Outcomes Following ACL Reconstruction With BTB Autograft
A NA study of ACL Reconstruction, sponsored by NYU Langone Health.
- Recruiting
- Registry status
- NA
- Development phase
- 90
- Enrollment target
- 1
- Study location
NCT06542705: Recruiting NA study of ACL Reconstruction, sponsored by NYU Langone Health.
NCT06542705 is a NA study of ACL Reconstruction that is actively recruiting participants, run by NYU Langone Health. The registered enrollment target is 90 participants, below the 111-participant average among 4 other ACL Reconstruction trials with a reported enrollment target (19% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06542705, a NA study of ACL Reconstruction, is actively recruiting participants, sponsored by NYU Langone Health.
- RECRUITING
- Registry status
- NA
- Development phase
- 90 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to assess Anterior Cruciate Ligament (ACL) healing through analyzing clinical, radiographic, functional and patient-reported outcomes following ACL reconstruction with bone-tendon-bone autograft with and without internal bracing.
Primary Outcome
The KT-1000 knee arthrometer (KT-1000) is an objective instrument to measure anterior tibial motion relative to the femur for anterior cruciate ligament (ACL) reconstruction. The side-to-side differences comparing the injured and normal extremity allow the determination of a diagnosis of increased anterior-posterior laxity. A side-to-side difference of less than 3mm at 30lb and the manual maximum is considered normal. A side-to-side difference between 3 and 5mm is considered a grey area. A side-
Conditions Studied
Interventions
- DEVICE Arthrex Internal Brace
- PROCEDURE ACL Reconstruction
Study Locations (1)
New York
- NYU Langone Health - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 90 participants |
| Start Date | 2025-03-17 |
| Est. Completion | 2029-03 |
| Phase | NA |
What NCT06542705 shows while recruiting
NCT06542705 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 90 participants, a relatively small participant target, below the 111-participant average among 4 other ACL Reconstruction trials with a reported enrollment target (19% lower).
The record links to 1 condition, with ACL Reconstruction appearing as the primary indexed condition, and to 2 interventions - of which Arthrex Internal Brace is the first listed.
NCT06542705 reports a single indexed study location in New York.
Frequently Asked Questions
What is clinical trial NCT06542705 about?
NCT06542705 is a clinical study titled "Effect of Internal Brace on Outcomes Following ACL Reconstruction With BTB Autograft". The purpose of this study is to assess Anterior Cruciate Ligament (ACL) healing through analyzing clinical, radiographic, functional and patient-reported outcomes following ACL reconstruction with bone-tendon-bone autograft with and without internal bracing.
What is the current status of trial NCT06542705?
This trial is currently recruiting. It is a NA study. The enrollment target is 90 participants. The study started on 2025-03-17. Estimated completion is 2029-03.
What conditions does trial NCT06542705 study?
This clinical trial studies the following conditions: ACL Reconstruction.
What interventions are being tested in trial NCT06542705?
The interventions under investigation include: Arthrex Internal Brace (DEVICE), ACL Reconstruction (PROCEDURE).
Who is sponsoring clinical trial NCT06542705?
This trial is sponsored by NYU Langone Health, which has 1,164 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06542705 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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