跳至主要内容
临床试验/CTRI/2024/06/068661
CTRI/2024/06/068661尚未招募3 期

Comparing erector spinae plane block and serratus anterior plane block for quality of recovery in patients posted for thoracotomy A prospective randomised double blinded controlled study

Dr Chandra Shekhar Kumar1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2024年7月1日最近更新:

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
120
试验地点
1
主要终点
Primary outcome is to assess quality of recovery using QOR-15 scale at 24 hours postoperatively.

研究概览

简要总结

A total of 120 thoracotomy patients have been equally divided into 2 groups(60 in each groups) receiving ESP and SAP blocks.Both group will receive 0.375% ropivacaine(0.5 ml/kg) with general anaesthesia.Patients included in our study are of age group between 18-70 years,ASA physical status 1-3,those willing to participate and able to comprehend.Patients excluded in our study are those allergic to local anaesthesia,chronic opioid use,infection at block site,cognitive dysfunction or psychiatric illness.We will compare ESP and SAP blocks and primary outcome will be to assess quality of recovery using QOR-15 scale at 24 hr postoperatively.and secondary outcome will be to assess post operative analgesia using NRS scale at 0,3,6,12,18 and 24 hours.

研究设计

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

入排标准

年龄范围
18.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • Patients age between 18-70 years of either sex Patients able to comprehend and willing to participate ASA physical status l-lll Patients scheduled to undergo for unilateral thoracotomy under general anaesthesia.

排除标准

  • Patients refusal to participate Allergy to local anaesthetics Chronic opioid use or history of chronic pain Infection at block site Cognitive dysfunction or psychiatric illness.

结局指标

主要结局

Primary outcome is to assess quality of recovery using QOR-15 scale at 24 hours postoperatively.

时间窗: Postoperative 24 hours

次要结局

  • To assess pain score using NRS scale upto 24 hours,time to rescue analgesia use,total analgesic consumption upto 24 hours,patients satisfaction and any adverse effects seen.(Pain score will be recorded at rest and during coughing using NRS scores at 0,3,6,12,18 and 24 hours.)

研究者

发起方
Dr Chandra Shekhar Kumar
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Chandra Shekhar kumar

Indira Gandhi Institute of Medical Sciences

研究点 (1)

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