To compare the outcome of total knee arthroplasty
Phase 4
- Conditions
- Health Condition 1: M170- Bilateral primary osteoarthritis of knee
- Registration Number
- CTRI/2019/11/021948
- Lead Sponsor
- Department Of OrthopaedicsAIIMSNew Delhi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1) Patient undergoing b/l total knee arthroplasty during study period using same implant
2)Varus deformity <30 degrees
3)Age between 50 years and 85 years
4)Patient having primary osteoarthritis
5)Patient giving consent for surgery
Exclusion Criteria
1) Revision cases of total knee arthroplasty
2) Post traumatic, post tb knee
3) patients with restricted range of motion <90 degrees
4) patients not giving consent
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Comparison of functional and patient reported outcome in cruciate retaining versus posterior stabilising total knee arthroplastyTimepoint: 12 months
- Secondary Outcome Measures
Name Time Method 1)To assess the FJS and OKS of cruciate retaining tkr <br/ ><br>2) To assess the FJS and OKS of posterior stabilising total knee arthroplastyTimepoint: 12 months