Status:

WITHDRAWN

Dynamic Splinting for Excessive Pronation Following CVA

Lead Sponsor:

Dynasplint Systems, Inc.

Conditions:

Pronation Contracture

Eligibility:

All Genders

18+ years

Phase:

NA

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.

Eligibility Criteria

Inclusion

  • Inclusion Criteria
  • Patients enrolled will have been diagnosed with excessive pronation following a stroke and will display the following symptoms:
  • Pronation Contracture
  • Ability to provide consent and follow directions as related to the protocol
  • Exclusion Criteria
  • Treatment with Benzodiazepines
  • Treatment with Baclofen (pump or oral)
  • Treatment with Dantrolene sodium
  • Treatment with Tizanidine

Exclusion

    Key Trial Info

    Start Date :

    May 1 2009

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    October 1 2016

    Estimated Enrollment :

    Patients enrolled

    Trial Details

    Trial ID

    NCT00900692

    Start Date

    May 1 2009

    End Date

    October 1 2016

    Last Update

    July 11 2013

    Active Locations (1)

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    Rehabilitation Associates of Indiana

    Indianapolis, Indiana, United States, 46250