跳至主要内容
临床试验/CTRI/2024/07/071108
CTRI/2024/07/071108尚未招募不适用

Efficacy of bilateral external oblique intercostal plane block for postoperative pain relief in patients undergoing laparoscopic cholecystectomy.

Pt BD Sharma PGIMS Rohtak1 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2024年8月2日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
44
试验地点
1
主要终点
To evaluate analgesic consumption (tramadol and paracetamol) in the first 24 hours in both groups.

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • 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.

排除标准

  • 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.

结局指标

主要结局

To evaluate analgesic consumption (tramadol and paracetamol) in the first 24 hours in both groups.

时间窗: To evaluate analgesic consumption(tramadol and paracetamol) at 30 mins, 1hr, 2hr,6hr, 12hr and 24hrs post operatively in both groups.

次要结局

  • 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.)

研究者

发起方
Pt BD Sharma PGIMS Rohtak
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Mamta Bhardwaj

Department of Anaesthesiology , Pandit BD Sharma PGIMS Rohtak.

研究点 (1)

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