se of the ROSA Knee Robot System for patients undergoing a primary total knee replacement - an early evaluation of the ROSA Knee System.

Not Applicable

Completed

• Conditions: Degenerative Joint Disease; Musculoskeletal - Other muscular and skeletal disorders; Musculoskeletal - Osteoarthritis; Surgery - Surgical techniques

• Registration Number: ACTRN12618000990224
• Lead Sponsor: Zimmer Biomet Pty Ltd

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2018-06-13
• Study Completion: 2019-09-02
• Last Update Posted: 10 February 2020

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 64

Inclusion Criteria

Patient qualifies for a primary total knee arthroplasty based on the investigator’s clinical judgement
Independent of study participation, patient is a candidate for commercially available Persona Total Knee or Vanguard Total Knee or NexGen Total Knee arthroplasty

Exclusion Criteria

Patient has active, local infection or previous intra-articular infection in the affected joint
Insufficient bone stock on femoral or tibial surfaces
Neuropathic arthroplasty
Osteomalacia or any metabolic disorder which may impair bone formation
Severe instability secondary to the absence of collateral ligament integrity
Rheumatoid arthritis accompanied by an ulcer of the skin or history of recurrent breakdown of the skin

Study & Design

• Study Type: Interventional
• Study Design: Not specified