A Prospective Cohort Post Market Registry Evaluating Outcomes of Bridge-Enhanced ACL Restoration (BEAR®)

Running, not enrolling

Conditions studied: Anterior Cruciate Ligament Injuries

In brief

The purpose of the Bridge Registry is to assess real-world performance of the FDA approved BEAR Implant.

Key facts

Study ID

NCT05398341

Run by

Miach Orthopaedics

People needed

300

Starts

2023-02-28

Expected to finish

2027-01-30

Last updated by the study team

2026-06-09

Who can join

Age: 14 and older. Sex: any. Healthy volunteers: not accepted.

You may not qualify if…

• The subject is participating in another ACL trial or any other clinical trial where the study procedure or treatment might confound the study end point
• Known allergy to bovine collagen, bovine gelatin or other bovine-derived products as contraindicated in the BEAR Implant labeling

Where it is running

• Stanford — Redwood City, California, United States
• Steamboat Orthopaedic and Spine Institute — Steamboat Springs, Colorado, United States
• Advent Health — Orlando, Florida, United States
• Virtua Health — Marlton, New Jersey, United States
• Hospital for Special Surgery — New York, New York, United States
• Victory Sports Medicine — Skaneateles, New York, United States
• Duke University — Durham, North Carolina, United States
• Oregon Health & Science University (OHSU) — Portland, Oregon, United States

Full record on ClinicalTrials.gov

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