PMCF Study on PEEK Suture Anchors for Hip Indications

Smith & Nephew

Status: Completed

Conditions: Soft Tissue to Bone Fixation

Treatments: Device: PEEK Suture Anchors

Study type: Observational

Funder types: Industry

Identifiers

NCT03814044

2018.14.SMD.PEEK.RET.HIP

Details and patient eligibility

About

Post-market clinical follow-up (PMCF) on the PEEK Suture Anchors in the hip.

Enrollment: 149 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Subjects who have undergone hip joint repair using the study devices.
2. Subjects aged 18 years and older at the time of surgery.
3. Subjects who had a visit to their provider between 3 and 15 months postoperative.

Exclusion criteria

1. Subjects who are < 12 months post-operative.
2. Subject is entered in another investigational drug, biologic, or device study or has been treated with an investigational product within 30 days prior to surgery
3. Subject had off-label use of the PEEK suture anchor during surgery.

Trial design