NCT00575458CompletedNot Applicable
Prospective Randomized Comparison of Dynamic Versus Static Splinting After Dupuytren's Contracture Release
Massachusetts General Hospital1 site in 1 country60 target enrollmentStarted: June 2005Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Enrollment
- 60
- Locations
- 1
- Primary Endpoint
- DASH questionnaire, PCS questionnaire, Wahler Physical Symptom Inventory, CESD questionnaire
Study Overview
Brief Summary
This study is comparing two different kinds of splints for patients who have had a surgical contracture release of dupuytren's disease. It compares a static splint and a dynamic splint.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •18 years or older
- •males and females with Dupuytren's contracture
- •patients with contracture of less than 30 degrees of MCP contractions and no contractions of the IP joints
Exclusion Criteria
- •previous surgical treatment for Dupuytren's
- •contracture of MCP greater than 30 degrees
- •contraindications for dynamic splinting (upper limb amputees, paresis, ect.)
Outcomes
Primary Outcomes
DASH questionnaire, PCS questionnaire, Wahler Physical Symptom Inventory, CESD questionnaire
Time Frame: 6 months
Secondary Outcomes
No secondary outcomes reported
Investigators
Study Sites (1)
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