跳至主要内容
临床试验/CTRI/2024/06/069307
CTRI/2024/06/069307尚未招募不适用

A comparative evaluation of ultrasound guided pudendal nerve block for postoperative analgesia in patients undergoing stapled hemorrhoidectomy.

未提供1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2024年7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
70
试验地点
1
主要终点
Time of requirement of first rescue opioid analgesic.

研究概览

简要总结

This is a clinical study designed to judge the efficacy of pudendal nerve block in patients undergoing stapled hemorrhoidectomy. This surgery is painful and use of regional analgesia technique as a part of multimodal analgesia regime is helpful for early rehabilitation of patient.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Investigator 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 undergoing stapled hemorrhoidectomy under GA • American society of anesthesiology (ASA) grade 1 and 2 patients.

排除标准

  • Patient refusal
  • ASA 3 and above
  • Patients with features of local infection at the site of block
  • Patients with history of bleeding disorder or on anticoagulant therapy
  • Patients with known allergy to local anesthetic drugs
  • Patients with mental illness
  • Patients with neuromuscular disorders.

结局指标

主要结局

Time of requirement of first rescue opioid analgesic.

时间窗: 0 , 4 , 8 ,12 and 24 hours

次要结局

  • 1. To compare overall requirements for Opioids in 24 hours.(2. Pain score.)

研究者

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

Dr Divesh Arora

Asian Hospital Faridabad

研究点 (1)

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