Efficacy of local anaesthesia in total knee replacement Surgeries
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2021/08/035366
- Lead Sponsor
- Dr Fatima khan
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1) ASA grade I - III
2) Patient giving written informed consent
3) Patient undergoing unilateral total knee replacement under spinal
Exclusion Criteria
1) Patient refusal
2) Patient would be excluded if they had a primary constrained prosthesis,
secondary arthritis due to rheumatoid arthritis or trauma, osteonecrosis or
revision surgery
3) Patient allergic to study medication,
4) ASA >III,
5) Contraindication for spinal anesthesia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To measure pain control using VAS score <br/ ><br>Timepoint: At 1hr, 2hr, 4hr, 6hr, 12hr, 24hr
- Secondary Outcome Measures
Name Time Method to measure functional recovery after surgery. <br/ ><br> Complications or side effects, if any. <br/ ><br>Timepoint: <br/ ><br> At day 1,day 3 , day 6 <br/ ><br>