A 4-Anchor Construct With Internal Bracing Technique for Surgical Treatment of Perilunate Dislocations
Part of paid clinical trials in Orlando, Florida.
- Sponsor
- Bryan D Brown,MD
- Study ID
- NCT07068893
- Status
- Recruiting
Conditions
- Perilunate Dislocation
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 88 Years
- Healthy Volunteers
- Not accepted
Study Details
The purpose of the research study is to determine the overall clinical and radiographic outcome differences between internal brace technique and the gold standard Kirschner wires (K-wire) technique for treatment of perilunate dislocations (e.g. nonunion, reoperation, infection, fixation failure, etc.). A secondary purpose is to determine the specific types of complications and their incidence rates with respect to internal brace technique and the gold standard Kirschner wires (K-wire) technique (e.g. range of motion losses, pain, numbness, weakness, etc).
Key Dates
- Start date
- Sep 17, 2025
- Status verified
- Dec 2025
- Primary completion
- Jan 31, 2028
- Completion
- Jan 31, 2028
Study Design
- Enrollment
- 40 participants (estimated)
Arms
- Arm: Patients who undergo traditional fixation
- Arm: Patients who undergo fixation using a novel 4-anchor construct with internal bracing
Primary Outcome Measure
Clinical Functional Assessment [ Time Frame: From enrollment to 2-years postoperative ]
Central Contacts
- Bryan Brown, MD321-890-7154
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Orlando Health | Orlando | Florida | 32806 |
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