The enrolment of Total Hip (THA), Total Knee (TKA) or Partial Knee Arthroplasty (PKA) patients performed using either Stryker Mako Robotic-Arm Assisted Technology (Mako) or non-Mako techniques into an outcomes data registry.

Not Applicable

• Conditions: Total Knee Arthroplasty; Partial Knee Arthroplasty; Total Hip Arthroplasty; Musculoskeletal - Osteoarthritis; Surgery - Surgical techniques

• Registration Number: ACTRN12622000370707
• Lead Sponsor: Stryker Australia Pty Ltd

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2022-03-02
• Last Update Posted: 7 March 2022

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 500

Inclusion Criteria

1. Patient has undergone or is to undergo a THA, TKA or PKA executed or to be executed via Mako or non-Mako techniques
2. Patient is a skeletally mature male or skeletally mature non-pregnant female aged 21 years or older at the time of consent
3. Patient has completed or is willing to complete the HREC-approved consent sign off via the myrecovery app

Exclusion Criteria

1. Patient has a cognitive impairment, an intellectual disability or a mental illness that is thought by the Investigator to impact on their ability to comply with the requirements of the study
2. Patient is unwilling to complete the consent sign off via the myrecovery app
3. Patient has had revision/reconstruction of THA, TKA or PKA. Only primary surgeries will be included in this registry.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
To compare the restoration of normal feeling of patients operated via Mako and non-Mako techniques. This will be achieved by employing the following instrument, Forgotten Joint Score.[Post-operative: 6 weeks, 1 year (primary timepoint), 2 years];To compare the postoperative satisfaction of patients operated via Mako and non-Mako techniques. This will be achieved by employing the following instrument, Net Promoter. [Post-operative: 6 months];To compare the postoperative satisfaction of patients operated via Mako and non-Mako techniques. This will be achieved by asking patients one question on how satisfied they are with their procedure. This questionnaire was designed specifically for this study.[Post-operative: 6 months, 1 year (primary timepoint), 2 years]