跳至主要内容
临床试验/CTRI/2024/08/072126
CTRI/2024/08/072126尚未招募不适用

Peri-anal block for post-operative analgesia in peri-anal surgery under spinal anaesthesia- A prospective randomized placebo-controlled trial.

Dr Shruti Priya1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2024年8月25日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
100
试验地点
1
主要终点
To compare time of first analgesia requirement in minutes when NRS greater than 4

研究概览

简要总结

Patient discomfort is exacerbated by postoperative pain, which increases the length of time spent in the ambulatory care unit. Post-operative pain management may be assisted by non-pharmacological therapies during the perioperative period. The pudendal nerve innervates the urethral muscles, clitoris, penis, and perineum.

Thus, we hypothesise that post-operative peri-anal block with 40 ml of 0.25% bupivacaine and dexmedetomidine (0.5 mg/kg) will provide effective and prolonged post-operative analgesia.

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
15.00 Year(s) 至 78.00 Year(s)(—)
性别
All

入选标准

  • Posted for electric peri-anal surgeries like fistula-in-ano, fissure, pilonidal sinus.
  • Surgery under spinal anaesthesia.

排除标准

  • Patient refusal.
  • Allergy to study drugs.
  • Acute peri-anal abscess and anorectal cancer.
  • Failed spinal block.
  • Inability to understand patient information leaflet and NRS score.

结局指标

主要结局

To compare time of first analgesia requirement in minutes when NRS greater than 4

时间窗: In postoperative at interval of just after surgery-1hr-2hr-4hr-8hr.

次要结局

  • 1. To compare total dose of analgesic requirement in term of morphine equivalent(2. To compare patient satisfaction score after surgery.)

研究者

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

Dr Shruti Priya

Indira Gandhi Institute of Medical Sciences

研究点 (1)

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