Dynamic Splinting for Excessive Pronation Following CVA

Not Applicable

Withdrawn

• Conditions: Pronation Contracture
• Interventions: Device: Dynasplint

• Registration Number: NCT00900692
• Lead Sponsor: Dynasplint Systems, Inc.

Brief Summary

The purpose of this study is to examine range of motion and lasting effects of Botox injections along with the use of the Supination Dynasplint.

Detailed Description

Not available

Study Timeline

• Study Start: 2009-05
• Study First Submitted: 2009-05-12
• Study First Submitted QC: 2009-05-12
• Study First Posted: 2009-05-13
• Status Verified: 2013-07
• Last Update Submitted: 2013-07-10
• Last Update Posted: 2013-07-11
• Primary Completion: 2016-09
• Study Completion: 2016-10

Recruitment & Eligibility

• Status: WITHDRAWN
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Dynasplint Group	Dynasplint	Along with the standard of care Botox and manual therapy, patients will use the Supination Dynasplint every day

Primary Outcome Measures

Name	Time	Method
ROM changes with use of treatment	20 weeks

Trial Locations

Locations (1)

Rehabilitation Associates of Indiana; 🇺🇸 Indianapolis, Indiana, United States