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Evaluation of Healing Following Open Gluteus Medius Repair With Biointegrative Implant

NCT05492396 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 30

Last updated 2026-04-01

No results posted yet for this study

Summary

This is a prospective, single-center study design with enrollment of 15 subjects. The 15 subjects will all undergo standard gluteus medius repair that includes augmentation with the biointegrative implant. This is a small observational study. As such, we expect that the results from 15 subjects will give an adequate understanding of post surgical healing.

Conditions

  • Hip Injuries
  • Tendon Injuries
  • Orthopedic Procedures

Interventions

DEVICE

Standard gluteus medius repair with Tapestry Biointegrative implant

Patients will undergo standard gluteus medius repair utilizing augmentation.

Sponsors & Collaborators

  • Ohio State University

    lead OTHER

Principal Investigators

  • William K Vasileff, MD · Ohio State University

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-08-01
Primary Completion
2025-06-25
Completion
2027-01-31
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05492396 on ClinicalTrials.gov