Efficacy of bilateral external oblique intercostal plane block for postoperative pain relief in patients undergoing laparoscopic cholecystectomy.
Overview
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Pt BD Sharma PGIMS Rohtak
- Enrollment
- 44
- Locations
- 1
- Primary Endpoint
- To evaluate analgesic consumption (tramadol and paracetamol) in the first 24 hours in both groups.
Overview
Brief Summary
Title of Study-Efficacy of bilateral external oblique intercostal plane block for postoperative pain relief in patients undergoing laparoscopic cholecystectomy.
44 patients (22 in each group), aged between 18-65 years belonging to ASA I & II scheduled to undergo laparoscopic cholecystectomy under general anaesthesia will be enrolled to compare the effect of external oblique intercostal plane block (EOIPB) and patient receiving standard multimodal analgesia. Analgesic consumption in first 24 hours, post op pain score evaluation using visual analogue scale in PACU, Time of first analgesic request, post op nausea and vomiting (PONV), sedation score, total intra operative fentanyl consumption, number of dermatomes anaesthetised, adverse effects (if any) will also be compared.
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Masking
- None
Eligibility Criteria
- Ages
- 18.00 Year(s) to 65.00 Year(s) (—)
- Sex
- All
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.
Outcomes
Primary Outcomes
To evaluate analgesic consumption (tramadol and paracetamol) in the first 24 hours in both groups.
Time Frame: To evaluate analgesic consumption(tramadol and paracetamol) at 30 mins, 1hr, 2hr,6hr, 12hr and 24hrs post operatively in both groups.
Secondary Outcomes
- 1.Postoperative pain score evaluation using visual analogue scale (VAS) in PACU at 30 min, 1 h, 2h, 6h. 12h and 24h postoperatively(2.Time of first analgesic request.)
Investigators
Dr Mamta Bhardwaj
Department of Anaesthesiology , Pandit BD Sharma PGIMS Rohtak.