跳至主要内容
临床试验/CTRI/2025/10/096518
CTRI/2025/10/096518尚未招募不适用

A comparative evaluation of effectiveness of external oblique intercostal plane block and subcostal transversus abdominis plane block in enhancing post op analgesia in laparoscopic cholecystectomy.

未提供1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2026年11月1日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
60
试验地点
1
主要终点
Total tramadol consumption in first 24 postoperative hours

研究概览

简要总结

This randomized, double-blind clinical study aims to compare the analgesic efficacy of the External Oblique Intercostal Plane (EOIB) block and the Subcostal Transversus Abdominis Plane (TAP) block in patients undergoing elective laparoscopic cholecystectomy. Sixty adult patients (ASA I–II, aged 18–60 years) will be randomly allocated into two equal groups to receive either EOIB or subcostal TAP block under ultrasound guidance, in addition to standard multimodal analgesia. The primary outcome is total tramadol consumption in the first 24 postoperative hours. Secondary outcomes include intraoperative fentanyl requirement, hemodynamic stability, time to first rescue analgesic, postoperative VAS pain scores, patient satisfaction, and incidence of nausea, vomiting, or sedation. Data will be analyzed using appropriate statistical methods with p < 0.05 considered significant. This study seeks to determine which block provides superior postoperative analgesia and better patient comfort after laparoscopic cholecystectomy, thereby contributing to improved regional anesthesia practices in upper abdominal surgeries.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant, Investigator and Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Patients aged 18–60 years belonging to ASA I–II status, scheduled for elective laparoscopic cholecystectomy who provided written informed consent will be recruited for this trial.

排除标准

  • Patients who refuse to participate, who have Local infection at injection site, are known allergic to local anesthetic drugs, are having coagulopathy or receiving anticoagulant drugs, are pregnant or having neuromuscular and psychiatric disorders will be excluded from the study.

结局指标

主要结局

Total tramadol consumption in first 24 postoperative hours

时间窗: Total tramadol consumption in first 24 postoperative hours

次要结局

  • Intraoperative fentanyl requirement(0, 2, 4, 8, 12, and 24 hours)

研究者

发起方
未提供
责任方
Principal Investigator
主要研究者

DIVESH ARORA

Asian Hospital Faridabad

研究点 (1)

Loading locations...

相似试验