Assessment of outcomes after robot-arm assisted total knee replacement
Not Applicable
Completed
- Conditions
- Health Condition 1: M170- Bilateral primary osteoarthritis of knee
- Registration Number
- CTRI/2020/11/029018
- Lead Sponsor
- Sunshine Hospitals Gachibowli
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 90
Inclusion Criteria
All patients eligible for Bilateral simultaneous total knee arthroplasty for primary OA of the knee joint
These patients are consented for participation in this RCT, in which they will receive robotic-arm assisted total knee replacement surgery with different alignment strategies in both the knees (i.e one knee randomized to receive TKR with FUNCTIONAL ALIGNMENT, and the second knee to receive TKR with MECHANICAL ALIGNMENT)
Exclusion Criteria
Post-traumatic arthritis
Asymmetrical knee deformities
Unwilling to participate in the trial
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain assessment using the Visual Analogue Pain Scale (VAS Pain), recorded for each knee separatelyTimepoint: Pain assessment using the Visual Analogue Pain Scale (VAS Pain), recorded for each knee separately at 6 hours, 12 hours, 18 hours, 24 hours, 36 hours and 48 hours after surgery
- Secondary Outcome Measures
Name Time Method