Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

ACTIVE NOT RECRUITING

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

NCT05398341 · View on ClinicalTrials.gov ↗

Study Summary

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

Interventions

  • DEVICE The BEAR® Implant

Study Locations (9)

New York

  • Hospital for Special Surgery — New York
  • Victory Sports Medicine — Skaneateles

California

  • Stanford — Redwood City

Colorado

  • Steamboat Orthopaedic and Spine Institute — Steamboat Springs

Florida

  • Advent Health — Orlando

Massachusetts

  • Boston Children's Hospital — Boston

New Jersey

  • Virtua Health — Marlton

North Carolina

  • Duke University — Durham

Oregon

  • Oregon Health & Science University (OHSU) — Portland

Trial Details

FieldValue
Enrollment Target 300 participants
Start Date 2023-02-28
Est. Completion 2027-01-30

Sponsor

Miach Orthopaedics

4 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05398341

The ClinicalTrials.gov registry entry for NCT05398341 describes a study currently listed as active not recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 300 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Miach Orthopaedics, which has 4 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Anterior Cruciate Ligament Injuries appearing as the primary indexed condition, and to 1 intervention — of which The BEAR® Implant is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05398341 reports 9 study locations spanning 8 distinct geographic areas — top geographies include New York, California, Colorado. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05398341 about?

NCT05398341 is a clinical study titled "A Prospective Cohort Post Market Registry Evaluating Outcomes of Bridge-Enhanced ACL Restoration (BEAR®)". The purpose of the Bridge Registry is to assess real-world performance of the FDA approved BEAR Implant.

What is the current status of trial NCT05398341?

This trial is currently active not recruiting. The enrollment target is 300 participants. The study started on 2023-02-28. Estimated completion is 2027-01-30.

What conditions does trial NCT05398341 study?

This clinical trial studies the following conditions: Anterior Cruciate Ligament Injuries. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05398341?

The interventions under investigation include: The BEAR® Implant (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05398341?

This trial is sponsored by Miach Orthopaedics, which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05398341 being conducted?

This trial has 9 study locations across California, Colorado, Florida, Massachusetts, New Jersey. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial