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Clinical Trials/ACTRN12622000370707
ACTRN12622000370707
Not yet recruiting
未知

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.

Stryker Australia Pty Ltd0 sites500 target enrollmentMarch 2, 2022

Overview

Phase
未知
Intervention
Not specified
Conditions
Total Knee Arthroplasty
Sponsor
Stryker Australia Pty Ltd
Enrollment
500
Status
Not yet recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 2, 2022
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

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.

Outcomes

Primary Outcomes

Not specified

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