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Study details
Enrolling now

Effect of Internal Brace on Outcomes Following ACL Reconstruction With BTB Autograft

NYU Langone Health
NCT IDNCT06542705ClinicalTrials.gov data as of Apr 2026
Target enrollment

90

Study length

about 4 years

Ages

18–35

Locations

1 site in NY

What this study is about

Researchers are testing whether using an internal brace after ACL reconstruction with a bone-tendon-bone autograft improves outcomes. The trial will follow participants for 1475 days and aims to enroll approximately 90 people.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Undergo ACL Reconstruction
  • 2.Use Arthrex Internal Brace

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
Randomized & Blinded

You may get a placebo/standard care, and you won't know which.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Secondary: Change from Baseline in International Knee Documentation Committee (IKDC) Survey at Month 12 Post-Operation, Change from Baseline in International Knee Documentation Committee (IKDC) Survey at Month 24 Post-Operation, Change from Baseline in Lysholm Knee Scoring System Score at Month 12 Post-Operation, Change from Baseline in Lysholm Knee Scoring System Score at Month 24 Post-Operation, Change from Baseline in Visual Analogue Scale (VAS) - Pain Score at Month 12 Post-Operation, Change from Baseline in Visual Analogue Scale (VAS) - Pain Score at Month 24 Post-Operation