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Post-market study on the impact of surgical approach on total hip replacement outcome

Not Applicable
Conditions
Osteoarthritis
Surgery - Surgical techniques
Musculoskeletal - Osteoarthritis
Registration Number
ACTRN12616000806460
Lead Sponsor
The International Musculoskeletal Research Institute Incorporated
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
All
Target Recruitment
624
Inclusion Criteria

Any osteo-arthritic patient that presents to an Investigator for a routine hip replacement surgery and is able to provide informed consent.
Any patient able to complete the required patient reported outcome measures.
Any patient able to undergo the required radiological examinations.

Exclusion Criteria

Participants with difficulty in comprehending study protocol through written or verbal English
Participants who, in the opinion of the Investigator, have an existing condition that would compromise their participation and follow-up.
Concurrent pregnancy.
Participants who are known drug or alcohol abusers or with psychological disorders that could affect follow-up care or treatment outcomes.
Participants who are currently involved in any injury litigation claims.
Participants with chronic gait affecting neurological conditions (e.g. stroke, Parkinson’s, Multiple sclerosis).
Participants with congenital hip defects.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The primary outcome measure for this study is the influence of three different surgical techniques on participant health-related quality of life (HRQoL) as assessed by the EuroQol-5D-5L (EQ-5D).[Pre-operatively, 2 weeks, 6 weeks, 3 months, 12 months and 24 months post-operatively];Identification of hip-specific function using the Oxford Hip Score (OHS)[Pre-operatively, 2 weeks, 6 weeks, 3 months, 12 months and 24 months post-operatively]
Secondary Outcome Measures
NameTimeMethod
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