Comparison of three approaches for primary Total Hip Arthroplasty

Not Applicable

Recruiting

• Conditions: Osteoarthritis; Musculoskeletal - Osteoarthritis; Surgery - Surgical techniques

• Registration Number: ACTRN12617000272392
• Lead Sponsor: Western Health

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2017-02-22
• Last Update Posted: 6 June 2022

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 243

Inclusion Criteria

Primary osteoarthritis of the hip requiring total hip replacement

Exclusion Criteria

Prior bony procedures on hip
Indication for THA is fracture, malignancy or developmental dysplasia

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Patient reported outcome measures (Oxford Hip Score)[6 weeks, 6 months, 12 months and 24 months post THA];Visual Analogue Scale for pain[Pre-operatively then 6 weeks, 6, 12 and 24 months post-operatively]

Secondary Outcome Measures

Name	Time	Method
Composite:<br>Residual pain - using Visual Analogue Scale and locating site of pain (trochanteric, gluteal or groin)<br>Complications including dislocation, infection, revision - defined by complication recorded in the medical record, return to theatre or patient reports complication occurring on follow up questioning.[6 weeks, 6 months, 12 months and 24 months post THA]