ltrasound-guided pericapsular nerve group block following hip arthroplasty for postoperative analgesia
Phase 2
Completed
- Conditions
- Health Condition 1: O- Medical and SurgicalHealth Condition 2: M169- Osteoarthritis of hip, unspecified
- Registration Number
- CTRI/2023/10/058678
- Lead Sponsor
- Swami Rama Himalayan University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 56
Inclusion Criteria
Type of hip surgery- Total Hip Arthroplasty, Hemiarthroplasty, Revision Arthroplasty
American Society of Anaesthesiologist (ASA) physical status Grade I and II
Exclusion Criteria
Patient refusal for Regional Anaesthesia.
Known allergies to Local anaesthetics.
Bleeding disorders
Infection at local site
Severe Liver and kidney disfunction
BMI above 30 kg/m2
Inability to give informed consent
Inability to operate PCA pump
Psychiatric Disorder
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Post Operative pain relief using NRS scoring scaleTimepoint: 24 hours
- Secondary Outcome Measures
Name Time Method Total opioid consumption over 24 hours <br/ ><br>Duration of the first rescue analgesic used over 24 hours (time from PACU discharge to first requested analgesic) <br/ ><br>Ability to Straight Leg Raise without any assistance on post operative day (POD) 1. <br/ ><br>Any opioid related side effects within the first 24 hours <br/ ><br>Any block related side effects in the first 24 hours <br/ ><br>Patient satisfaction utilising a Likert-scale questionnaire on POD 1Timepoint: 24 HOURS