ltrasound guided dual subsartorial block versus ACB + IPACK for postoperative recovery profile after total knee replacement
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/08/072388
- Lead Sponsor
- Maulana Azad Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA physical status I, II & III undergoing unilateral total knee arthroplasty.
Exclusion Criteria
1. Any contraindication to spinal anaesthesia.
2. Infection at the site of block injection.
3. Any known history of allergy to local anaesthetics.
4. Patients on opioids for chronic pain.
5. Pregnancy and lactating women.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method mean duration of postoperative analgesiaTimepoint: time at which first rescue analgesia will be given <br/ ><br>(variable for each patient)
- Secondary Outcome Measures
Name Time Method mean time by TUG testTimepoint: 24 hours <br/ ><br>48 hours;mean patient satisfaction score by Likert scaleTimepoint: 24 hours <br/ ><br>48 hours;mean time to postoperative ambulationTimepoint: time to postoperative ambulation;mean total opioid consumption in first 24 hour of the blockTimepoint: 24 hours;MRC score for evaluation of postoperative quadriceps muscle strengthTimepoint: 6 hours <br/ ><br>12 hours <br/ ><br>24 hours <br/ ><br>48 hours;Percentage of people experiencing postoperative pain at site 1, 2a, 2b, 2c, 2d, 3 according to appendix IITimepoint: time to first rescue analgesia