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临床试验/CTRI/2024/12/078279
CTRI/2024/12/078279尚未招募4 期

Ultrasound-guided erector Spinae plane block versus ilioinguinal/iliohypogastric block for postoperative analgesia in patients undergoing inguinal surgeries : A randomised clinical trial

Dr Neha Chajgotra1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2025年1月1日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
100
试验地点
1
主要终点
1) Severity of pain using Numerical Rating Scale (NRS)

研究概览

简要总结

This study is a randomised, parallel group, clinical trial comparing the effectiveness of two blocks i.e ultrasound guided Erector Spinae plane block versus ilioinguinal/ iliohypogastric block for postoperative analgesia in patients undergoing inguinal surgeries, as measured by duration of analgesia and pain score in 24 hours following surgery. The primary outcome of the study is to record the severity of pain using Numerical rating scale and time to request of first analgesia i.e the time elapsed between the end of surgery to 1st dose of analgesia. The secondary outcome is to see the total no. of analgesic doses of opioids and NSAIDs in 24 hours following surgery and to see any side effects like nausea, vomiting and shivering occurring after the procedure.

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
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • patients between age group of 18 years to 60years who are undergoing inguinal hernia repair in elective OT 2) ASA class 1 & 2 3) patients who are willing to participate and provide a willing written informed consent.

排除标准

  • patients with any chronic medical illness 2) history of any bleeding disorders 3) patients allergic to any of these drugs.

结局指标

主要结局

1) Severity of pain using Numerical Rating Scale (NRS)

时间窗: Severity of pain using Numerical Rating Scale (NRS) at 1,2,6,12 and 24 hours after surgery

2) Time to 1st request of analgesia

时间窗: Severity of pain using Numerical Rating Scale (NRS) at 1,2,6,12 and 24 hours after surgery

次要结局

  • 1) Total number of analgesic doses of opioids and NSAIDS in 24 hours following surgery(2) side effects like nausea, vomiting and shivering)

研究者

发起方
Dr Neha Chajgotra
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Neha Chajgotra

Government Medical College Kathua

研究点 (1)

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