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Clinical Trials/NCT03183856
NCT03183856
Completed
Not Applicable

Comparison of Clinical Efficacy and Safety for Ambulatory and Functional Improvement in Patients After Total Knee Arthroplasty With Morning Walk

Ulsan University Hospital1 site in 1 country9 target enrollmentSeptember 15, 2017
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ConditionsArthroplasty, Replacement, KneeRobotics

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Arthroplasty, Replacement, Knee
Sponsor
Ulsan University Hospital
Enrollment
9
Locations
1
Primary Endpoint
Change of WOMAC index
Status
Completed
Last Updated
7 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

The aim of this study is to determine the clinical efficacy and feasability of gait rehabilitation robot through approving functional improvement by an end-effector typed gait robot in patients underwent total knee arthroplasty.

Detailed Description

pre-interventional evaluation; within 1 day of initiation of the intervention; 5 days after initiation of the intervention; 10 days after intervention after initiation of the intervention; 42 days after intervention start

Registry
clinicaltrials.gov
Start Date
September 15, 2017
End Date
May 25, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Chang Ho Hwang

PhD and MD

Ulsan University Hospital

Eligibility Criteria

Inclusion Criteria

  • •Patients underwent Unilateral or both Total Knee Arthroplasty

Exclusion Criteria

  • •brain disease, spinal cord injury, peripheral neuropathy, myopathy
  • •Inability to ambulate fully due to muscukoskeletal disorders
  • •history of arthroplasty surgery on either of legs
  • •Cardiac pacemaker
  • •Refusal of participation

Outcomes

Primary Outcomes

Change of WOMAC index

Time Frame: 1 day before the initiation of intervention), 5 day, 10 day, and 31 days after the initiation of intervention

Western Ontario and McMaster Universities Osteoarthritis Index

Secondary Outcomes

  • Change of VAS(1 day before the initiation of intervention), 5 day, 10 day, and 31 days after the initiation of intervention)

Study Sites (1)

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