PMCF Study on PEEK Suture Anchors for Hip Indications

NCT03814044 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 149

Last updated 2024-10-15

Study results available
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Summary

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

Conditions

  • Soft Tissue to Bone Fixation

Interventions

DEVICE

PEEK Suture Anchors

Subjects who have undergone hip joint repair using PEEK Suture Anchors: BIORAPTOR™ Knotless Suture Anchor and SpeedLock Hip Suture Anchor

Sponsors & Collaborators

  • Smith & Nephew, Inc.

    lead INDUSTRY

Principal Investigators

  • Judith Horner · Smith & Nephew, Inc.

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-05-10
Primary Completion
2019-09-10
Completion
2019-09-10

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 NCT03814044 on ClinicalTrials.gov