Active — Not RecruitingNot Applicable

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

United States300 participantsStarted 2023-02-28

Plain-language summary

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

Who can participate

Age range

14 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

. Scheduled to undergo ACL surgery with the BEAR Implant
. Willing and able to provide informed consent
. Willing and able to complete required follow-up visits and assessments

Exclusion criteria

. 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

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

International Knee Documentation Committee (IKDC) Subjective Knee Evaluation score at year 2

Timeframe: 2 Years

Knee laxity based on the Lachman test at 1 year

Timeframe: 1 year

Trial details

NCT IDNCT05398341

SponsorMiach Orthopaedics

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2026-10-30

View on ClinicalTrials.gov More Anterior Cruciate Ligament Injuries trials