Comparison Of Dual And Single Subsartorial Block For Pain Relief After Knee Replacement Surgery
Phase 4
- Conditions
- Health Condition 1: O- Medical and SurgicalHealth Condition 2: M179- Osteoarthritis of knee, unspecified
- Registration Number
- CTRI/2021/12/038736
- Lead Sponsor
- Baroda medical college
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients undergoing primary unilateral total knee arthroplasty under spinal anaesthesia
2. Patients of ASA I-III
3. Ability to follow study protocol
Exclusion Criteria
1. Inability or refusal to follow the study protocol.
2. Coagulopathy.
3. Pre-existing lower extremity neuromuscular disorders
4. Local infection over the injection site
5. Allergy or contraindications to the drugs used in the study (local anesthetics, NSAIDs, opioids).
6. Chronic opioid use
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Changes in Post operative pain intensity and pain control <br/ ><br> <br/ ><br>Timepoint: Assessed at 4 hours, 8 hours, 18 hours 24hours
- Secondary Outcome Measures
Name Time Method 1. Extent of motor Blockage <br/ ><br>2. Post-operative ability of early ambulation <br/ ><br>3. Rate of Patient satisfaction <br/ ><br>4. Rate of post-operative complications <br/ ><br>Timepoint: Assessed at 4 hours,8 hours, 18 hours and 24 hours