A monocentric, retrospective and prospective, non-randomised, clinical survey to evaluate Mpact cup performance 5 years following Total hip arthroplasty

Not Applicable

Completed

• Conditions: Osteoarthritis; Total Hip Arthroplasty; Musculoskeletal - Osteoarthritis; Surgery - Other surgery

• Registration Number: ACTRN12623000788673
• Lead Sponsor: Medacta Australia Pty Ltd

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2017-12-04
• Study Start: 2023-07-19
• Last Update Posted: 25 July 2023

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 52

Inclusion Criteria

• Patient who underwent THA from March 2011 till November 2011.
• Patient who received a Mpact cup.
• Patient who agrees to comply with the study protocol.
• Patient who gave their consent to the treatment of his/her clinical data

Exclusion Criteria

• Minor patient
• Pregnant or breast feeding woman
• Patient who is not able to provide consent for participation in the study.
• Patient refusing data collection

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Mean scores on patient reported outcome questionnaire - Modified Harris Hip Score (HSS) questionnaire to assess the functional capacity of the patient after surgery.[6 weeks, 3 months, 1, 2 and 5 years after surgery];Radiological Performance using standard x-rays to assess device status, based on bone fixation and placement.[6 weeks, 3 months, 1, 2 and 5 years after surgery]

Secondary Outcome Measures

Name	Time	Method
Incidence of device and/or surgical-associated complications collected from review of medical records such as loosening and wear.[5 years after surgery]