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Clinical Trials/NCT00857701
NCT00857701
Terminated
Not Applicable

Dynamic Splinting After Total Knee Arthroplasty: a Randomized, Controlled Trial

Dynasplint Systems, Inc.1 site in 1 country25 target enrollmentJanuary 2009
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ConditionsReduced Knee Flexion

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Reduced Knee Flexion
Sponsor
Dynasplint Systems, Inc.
Enrollment
25
Locations
1
Primary Endpoint
Change in Maximal Acitive Range of Mothion in knee extension
Status
Terminated
Last Updated
12 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

The purpose of this study is to evaluate the effectiveness of a dynamic splinting system for knee flexion contracture following a total knee arthroplasty.

Detailed Description

The purpose of the study is to evaluate the efficacy of dynamic splinting for knee flexion contracture following a total knee arthroplasty.

Registry
clinicaltrials.gov
Start Date
January 2009
End Date
May 2015
Last Updated
12 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • •Reduced flexibility in AROM of knee extension
  • •Pain that is worsened by bending over while legs are straight
  • •Impaired gait pattern
  • •Ability to understand informed consent and experiment responsibilities

Exclusion Criteria

  • •Fractures
  • •Knee sepsis
  • •Osteomyelitis or any orthopedic infection
  • •Extensor mechanism dysfunction
  • •Psoriasis
  • •Knee joint neuropathy
  • •Previous Stroke or Brain Injury

Outcomes

Primary Outcomes

Change in Maximal Acitive Range of Mothion in knee extension

Time Frame: 9 weeks

Study Sites (1)

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