Effect of intra-articular pain relief cocktail on post-operative functional outcome in Total Knee Replacement.
Phase 1
Completed
- Conditions
- Health Condition 1: M171- Unilateral primary osteoarthritisof knee
- Registration Number
- CTRI/2018/05/014183
- Lead Sponsor
- Armed Forces Medical College Pune
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 30
Inclusion Criteria
All patients with osteoarthritis of knee undergoing unilateral Total knee arthroplasty
Exclusion Criteria
Patients undergoing revision knee arthroplasty, patients with peripheral vascular disease in the affected limb, patients with deranged coagulation profile, patients with major neurological deficit and uncontrolled angina, patients operated under general anesthesia, patients with history of allergy to cocktail drugs under study, patients who are provided with any alternative method of post op pain relief except combined spinal epidural analgesia.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method