Safety and Performance of PEEK Anchors in Extremities

Completed

Conditions studied: Medial or Lateral Instability Repairs/Reconstructions, Hallux Valgus Repairs, Achilles Tendon Repairs/Reconstructions, Midfoot Reconstructions, Metatarsal Ligament/Tendon Repairs/Reconstructions, Bunionectomy, Scapholunate Ligament Reconstructions, Ulnar, Lateral Epicondylitis Repair, Bicep Tendon Reattachments

In brief

Safety and performance of the study devices in extremities up to 12 months post-surgery

Key facts

Study ID

NCT03782298

Run by

Smith & Nephew, Inc.

People needed

140

Starts

2019-03-12

Expected to finish

2019-10-10

Last updated by the study team

2024-10-01

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects who have undergone extremity joint repair using the study devices.
• Subjects aged 18 years and older at the time of surgery.

You may not qualify if…

• Subject is entered in another investigational drug, biologic, or device study or has been treated with an investigational product within 12 months post-operative.
• Subjects who are < 3 months post-operative

Where it is running

• OrthoCarolina — Charlotte, North Carolina, United States
• Precision Orthopaedic Specialties, Inc. — Chardon, Ohio, United States
• Foot and Ankle Associates of North Texas-Grapevine — Grapevine, Texas, United States
• Fowler Kennedy Sport Medicine Clinic — London, Ontario, Canada

Full record on ClinicalTrials.gov

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