se of regional blocks in hip replacement surgeries
Phase 4
- Conditions
- Health Condition 1: O- Medical and SurgicalHealth Condition 2: M161- Unilateral primary osteoarthritisof hip
- Registration Number
- CTRI/2022/12/047838
- Lead Sponsor
- Deepak Kumar Dwivedi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA-I,II and III
BMI between 18-35 kg/m2
Exclusion Criteria
inability to consent to the study, coagulopathy, sepsis, hepatic or renal failure, allergy to local anesthetic (LA), prior surgery of the inguinal or suprainguinal area, pregnancy, and opioid intake at home.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome would be quality of recovery, assessed using the Quality of Recovery-15 (QoR-15) scale8 at 24 h postoperatively.Timepoint: 24 h postoperatively.
- Secondary Outcome Measures
Name Time Method 1. Incidence of quadriceps motor block (defined as paresis or paralysis of knee extension) at 6 hours, 12 hours and 24 hrs postoperatively. <br/ ><br>2. Static (at rest) and dynamic (with hip adduction) pain scores (Numeric rating scale score 1-10) at 3, 6, 12, 24hr <br/ ><br>3. Performance timeTimepoint: Post operative period for 24 hours