Hip Arthroscopy Versus Total Hip Arthroplasty RCT

  • STATUS
    Recruiting
  • End date
    Oct 31, 2022
  • participants needed
    20
  • sponsor
    Western University, Canada
Updated on 26 January 2021
osteoarthritis
osteotomy
hip arthroplasty
hip replacement
joint reconstruction

Summary

The aim of the proposed study is to perform a comparative pilot, randomized controlled trial of hip arthroscopy versus definitive total hip replacement (THR) for the treatment of early hip osteoarthritis (Tnnis Grade 1-2) in patients between the ages of 40-60 years.

Description

The purpose of this pilot study is to determine study feasibility. Specifically, the investigators aim to:

  1. estimate the proportion of eligible patients providing consent,
  2. estimate the magnitude of the between-groups difference in the primary outcome (Hip Dysfunction and Osteoarthritis Outcome Score - HOOS) to aid in sample size calculation for the full study,
  3. estimate the compliance in completing the proposed outcome measures to determine the burden of questionnaire completion.

Details
Condition Osteoarthritis of hip, Osteoarthritis, Osteoarthritis, hip oa
Treatment Total Hip Arthroplasty, Hip Arthroscopy
Clinical Study IdentifierNCT04166227
SponsorWestern University, Canada
Last Modified on26 January 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Radiographic evidence of mild to moderate hip OA (Tnnis Gr 0 with MRI chondral wear, Tnnis Gr 1 and 2)
Patients must have completed 3 months of non-operative management with ongoing symptoms

Exclusion Criteria

Advanced OA, defined as <2 mm joint space (Tnnis Gr 3) or those with acetabular or femoral head cysts
Patients who are pregnant or may become pregnant around the time of surgery
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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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