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A Study of the Safety and Performance of the MINITAC◊ Titanium 2.0 Suture Anchor

NCT04186481 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 32

Last updated 2021-02-26

Study results available
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Summary

This is a retrospective study evaluating the safety and performance of the MINITAC Suture anchors for extremities repair. Data will be used to support Notified Body (BSI) requirements for extremities repair indications.

Conditions

  • Hallux Valgus Repairs
  • Medial or Lateral Instability Repairs/Reconstructions
  • Achilles Tendon Repairs/Reconstructions
  • Midfoot Reconstructions
  • Metatarsal Ligament/Tendon Repairs/Reconstructions
  • Scapholunate Ligament Reconstructions
  • Ulnar or Radial Collateral Ligament Reconstructions
  • Lateral Epicondylitis Repair
  • Biceps Tendon Reattachment

Interventions

DEVICE

MINITAC Ti 2.0 suture anchor

The MINITAC◊ Ti 2.0 Suture Anchor is intended to provide secure reattachment of soft tissue to bone in the foot and ankle as well as elbow, wrist and hand.

Sponsors & Collaborators

  • Smith & Nephew, Inc.

    lead INDUSTRY

Principal Investigators

  • Thomas Thorvaldson, B.Med.Sc (Syd), B.Med.(Newc) · Maitland Hand and Othopaedic surgery

  • Stephan Mangin · Clinical Director, Global Clinical Strategy, Sports Med and ENT Smith & Nephew

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-10-25
Primary Completion
2019-11-08
Completion
2019-11-08

Countries

  • Australia

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 NCT04186481 on ClinicalTrials.gov