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Wrist Extension Dynasplint (WED) Distal Radius Fracture

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified April 2012 by Dynasplint Systems, Inc..
Recruitment status was:  Not yet recruiting
ClinicalTrials.gov Identifier:
First Posted: May 2, 2012
Last Update Posted: May 2, 2012
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Dynasplint Systems, Inc.
The purpose of this study is to evaluate the effectiveness of a dynamic splinting system for wrist extension contracture following a distal radius fracture.

Condition Intervention
Distal Radius Fracture Wrist Contracture Device: Wrist Extension Dynasplint

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Contracture Reduction Following Distal Radius Fracture

Resource links provided by NLM:

Further study details as provided by Dynasplint Systems, Inc.:

Primary Outcome Measures:
  • Change in maximal active range of motion in wrist extension [ Time Frame: 12 weeks ]

Estimated Enrollment: 50
Estimated Study Completion Date: December 2016
Estimated Primary Completion Date: December 2016 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: experimental
Patients will be treated with the Standard of Care physical therapy, NSAIDs as well as a Wrist Extension Dynasplint
Device: Wrist Extension Dynasplint
Dynamic Splinting utilizes the protocols of Low-Load, Prolonged-Duration Stretch (LLPS) with calibrated, adjustable tension to increase the Total End Range Time (TERT) to reduce contracture. The Knee Extension Dynasplint for the Experimental group will have tension chambers delivering therapeutic treatment from the device.
No Intervention: Control
Patients will receive standard of care physical therapy and NSAIDS


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 80 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Distal radius fracture treated with surgical management and wrist flexion contracture upon follow up

Exclusion Criteria:

  • Carpal Fractures (Scaphoid, Lunate, Hamate, and Trapezium)
  • Radial nerve entrapment
  • Arthrodesis
  • Traumatic dislocation of the distal ulna
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01589627

Sponsors and Collaborators
Dynasplint Systems, Inc.
Principal Investigator: Stacy Berner, MD Advanced Centers for Orthopaedic Surgery and Sports Medicine
  More Information

Responsible Party: Dynasplint Systems, Inc.
ClinicalTrials.gov Identifier: NCT01589627     History of Changes
Other Study ID Numbers: 2009.003
First Submitted: April 27, 2012
First Posted: May 2, 2012
Last Update Posted: May 2, 2012
Last Verified: April 2012

Keywords provided by Dynasplint Systems, Inc.:
distal radius fracture
wrist contracture

Additional relevant MeSH terms:
Fractures, Bone
Radius Fractures
Wounds and Injuries
Forearm Injuries
Arm Injuries
Joint Diseases
Musculoskeletal Diseases
Muscular Diseases