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Safety and Performance of the SUTUREFIX ULTRA and SUTUREFIX CURVED Suture Anchors in Shoulder and Hip Arthroscopic Repair

NCT03691298 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 83

Last updated 2025-01-06

Study results available
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Summary

The scientific justification is to fulfill post-market clinical requirements in order to support re-certification of the CE-Mark for this marketed product and to look into safety and efficacy.

Conditions

  • Instability, Joint

Interventions

DEVICE

SUTUREFIX ULTRA Suture Anchor and SUTUREFIX CURVED Suture Anchor

Fixation device intended to provide secure fixation of soft tissue to bone

Sponsors & Collaborators

  • Smith & Nephew Orthopaedics AG

    lead INDUSTRY

Principal Investigators

  • Laura Everson · Smith & Nephew Ltd

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-11-07
Primary Completion
2021-05-21
Completion
2021-05-21

Countries

  • United States
  • Denmark
  • Finland
  • Italy
  • Spain
  • United Kingdom

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 NCT03691298 on ClinicalTrials.gov