A comparative study between two lower limb nerve blocks in post operative bilateral total knee replacement patients.
Phase 2
- Conditions
- Health Condition 1: null- ASA I,II AND IIIHealth Condition 2: M170- Bilateral primary osteoarthritis of knee
- Registration Number
- CTRI/2018/05/013680
- Lead Sponsor
- Department of Anaesthesiology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Age more than 50 years of either sex
2.ASA- I, II and III
3.Patients undergoing primary Bilateral total knee arthroplasty
Exclusion Criteria
1] Associated coagulation disorders
2] Severe cardiac, renal or hepatic dysfunction
3] Allergy to TEST drug
4] Any pre-existing sensory or motor impairment
5] Patient refusal/chronic pain medications
6] Patient with cognitive impairment
7] Patient unable to understand study protocol and VAS scoring
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess the post-operative analgesia of adductor canal block and femoral nerve block in bilateral total knee arthroplasty with Visual Analog Scale.Timepoint: within 48hrs of post operative period
- Secondary Outcome Measures
Name Time Method 1.To assess the degree of quadriceps muscle weakness in post total knee arthroplasty in both methods. <br/ ><br>2.To assess the degree of knee flexion in post total knee arthroplasty in both methods. <br/ ><br>3.To compare complications if any, in either method. <br/ ><br> <br/ ><br>Timepoint: With in 48hrs of post operative period <br/ ><br> <br/ ><br>