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Clinical Trials/NCT02032017
NCT02032017
Unknown
N/A

Percutaneous Assisted Approach for Total Hip Replacement and it's Effect on Functional Rehabilitation Compared to the Anterolateral Approach.

Universiteit Antwerpen2 sites in 1 country30 target enrollmentOctober 2013

Overview

Phase
N/A
Intervention
Not specified
Conditions
Total Hip Arthroplasty
Sponsor
Universiteit Antwerpen
Enrollment
30
Locations
2
Primary Endpoint
change in time needed for the timed get up and go test
Last Updated
12 years ago

Overview

Brief Summary

The purpose of this study is to investigate whether revalidation following total hip replacement through the percutaneous approach is faster or better than following the anterolateral approach. We assume this would be the case since it is possible to spare a large part of the gluteus medius muscle with the percutaneous approach.

Registry
clinicaltrials.gov
Start Date
October 2013
End Date
December 2014
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Claudia Hendrickx

PhD student

Universiteit Antwerpen

Eligibility Criteria

Inclusion Criteria

  • unilateral hip arthritis or avascular necrosis (AVN) in need for total hip replacement

Exclusion Criteria

  • Comorbidities affecting functional outcome
  • Symptomatic lumbar pathology
  • Need of surgery or intervention on the ipsilateral knee and/or ankle/foot
  • Neurological disorders such as Parkinsonism and previous cardiovascular accidents (CVA)

Outcomes

Primary Outcomes

change in time needed for the timed get up and go test

Time Frame: baseline, 4 weeks, 12 weeks

The subject is asked to stand up from a chair, walk 3m to a cone, return to the chair and sit down again. The time needed to perform this test is recorded in seconds.

Secondary Outcomes

  • surface electromyography (sEMG) of gluteus medius(12 weeks)
  • Change in hip abductor muscle strength measured by MicroFET 2(baseline, 4 weeks, 12 weeks)
  • Change in time needed to complete the 5 times sit-to-stand test(baseline, 4 weeks, 12 weeks)
  • Change in distance walked during the 6 minute walking test(baseline, 4 weeks, 12 weeks)
  • Score on the trendelenburg test(4 weeks)
  • Change in knee extensor muscle strength measured by MicroFET 2(baseline, 4 weeks, 12 weeks)
  • Score on the Trendelenburg test(12 weeks)
  • Change in score on the Oxford Hip Score(baseline, 4 weeks, 12 weeks)
  • Change in score on the SF-36 and it's subscales(baseline, 4 weeks, 6 weeks)

Study Sites (2)

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