Status:
TERMINATED
Adhesive Capsulitis and Dynamic Splinting
Lead Sponsor:
Dynasplint Systems, Inc.
Conditions:
Adhesive Capsulitis
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The purpose of this study is to examine the efficacy of dynamic splinting in reducing contracture following diagnosis of adhesive capsulitis.
Detailed Description
This randomized controlled trial will explore the efficacy of dynamic splinting in conjunction with the current standard of care as compared to standard of care alone.
Eligibility Criteria
Inclusion
- Greater than 25% reduction in maximal external rotation plus greater than 25% reduction in at least one other plane of motion (elevation or abduction), as compared to the asymptomatic shoulder, measure supine with humerus abducted to 90º
- Duration from onset less than 12 months.
- Pain that is worsened by moving the arm in that direction
Exclusion
- Any previous shoulder surgery.
- Brachial plexus injuries
- Neurologically mediated pain and fibromatosis-like contracture
- Concomitant neurologic complaints or abnormalities
- Glenohumeral impingement or mechanical blockage
- Oncological process affecting the shoulder
- Previous total mastectomy
- Glenohumeral arthritis
Key Trial Info
Start Date :
January 1 2013
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
Estimated Enrollment :
5 Patients enrolled
Trial Details
Trial ID
NCT01874821
Start Date
January 1 2013
Last Update
August 12 2013
Active Locations (1)
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1
New York University
New York, New York, United States, 10003