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临床试验/CTRI/2024/03/063808
CTRI/2024/03/063808尚未招募2 期

Comparison of ultrasound guided erector spine block and oblique subcoastal transverse abdominis block for postoperative analgesia after laproscopic cholecystectomy

Bangalore medical college and research institute1 个研究点 分布在 1 个国家目标入组 140 人开始时间: 2024年3月15日最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
140
试验地点
1
主要终点
Duration of analgesia in 24 hour post operative period.

研究概览

简要总结

Laproscopic cholecystectomy ispreferred surgery due to its minimal invasive nature. Despite of being minimal invasive procedure it produces significant postoperative pain. Multimodal  approach to postoperative pain management include local infiltration, peripheral nerve block’ neuroaxial analgesia, analgesic drugs with different mechanism that gives synergistic effect on pain management.

Ultrasound guided erector spinae plane block ( ESPB) block mainly acts on both ventral and dorsal rami and rami communicantes of spinal nerve hence effective on both visceral and somatic pain.

Oblique subcoastal transverse abdominis plane block (OSTAPB) is modification of transverse abdominis plane block(TAP) and is recently described regional analgesia technique for supraumbilicalsurgeries like laproscopic cholecystectomy.

This study is designed to compare ultrasound guided ESPB and OSTAPB for postoperative analgesia after laproscopic cholecystectomy.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant Blinded

入排标准

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

入选标准

  • Patients willing to give informed consent
  • Patients aged between 21-60 years of age of either gender.
  • Patients of ASA Grade I and ASA Grade II
  • Patients undergoing elective laproscopic chlolecystectomy.

排除标准

  • 未提供

结局指标

主要结局

Duration of analgesia in 24 hour post operative period.

时间窗: Duration of analgesia in 24 hour post operative period.

次要结局

  • Post operative rescue analgesia requirement for 24 hours.(evaluate the adverse effects of both the blocks)

研究者

发起方
Bangalore medical college and research institute
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Manisha Singh M S

Bangalore medical college and research institute

研究点 (1)

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