Trials / Completed
CompletedNCT04186481
A Study of the Safety and Performance of the MINITAC◊ Titanium 2.0 Suture Anchor
Safety and Performance of MINITAC◊ Ti 2.0 Suture Anchor in Extremities
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 32 (actual)
- Sponsor
- Smith & Nephew, Inc. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
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.
Detailed description
Up to 3 sites will participate in the study across Australia and the EU, collectively enrolling a minimum of 30 and a maximum of 50 subjects into the study.
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
| Type | Name | Description |
|---|---|---|
| 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. |
Timeline
- Start date
- 2019-10-25
- Primary completion
- 2019-11-08
- Completion
- 2019-11-08
- First posted
- 2019-12-04
- Last updated
- 2021-02-26
- Results posted
- 2021-02-26
Locations
1 site across 1 country: Australia
Source: ClinicalTrials.gov record NCT04186481. Inclusion in this directory is not an endorsement.