To see the effect of external oblique intercostal plane block on post operative pain relief in patients for laparoscopic cholecystectomy.
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/07/071108
- Lead Sponsor
- Pt BD Sharma PGIMS Rohtak
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
American society of Anesthesiologists (ASA) physical status I to II, scheduled to undergo Laparoscopic cholecystectomy (LC) under general anaesthesia will be included in the study.
Exclusion Criteria
Patients with allergy to local anaesthetics, coagulopathies, pregnancy, infection at local site, weight less than 45kg and BMI more than 35 kg/m², chronic opioid use, history of abdominal surgery, refusal to consent.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate analgesic consumption (tramadol and paracetamol) in the first 24 hours in both groups.Timepoint: To evaluate analgesic consumption(tramadol and paracetamol) at 30 mins, 1hr, 2hr,6hr, 12hr and 24hrs post operatively in both groups.
- Secondary Outcome Measures
Name Time Method 1.Postoperative pain score evaluation using visual analogue scale (VAS) in PACU at 30 min, 1 h, 2h, 6h. 12h and 24h postoperatively <br/ ><br>2.Time of first analgesic request. <br/ ><br>3.Postoperative Nausea and Vomiting (PONV) <br/ ><br>4.Sedation score <br/ ><br>5.Number of dermatomes anaesthetised. <br/ ><br>6.Adverse effects (if any) <br/ ><br>Timepoint: At 30 min, 1h, 2h, 6h. 12h and 24h postoperatively.