跳至主要内容
临床试验/CTRI/2024/01/061389
CTRI/2024/01/061389尚未招募4 期

A Randomized controlled trial on efficacy of single dose of intraoperative dexamethasone in reducing post operative pain in caesarean section

All indian institute of medical sciences0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

入选标准

  • All pregnant women aged 18 to 40 years undergoing caesarean section
  • 1. Willing to give written informed consent
  • 2. Elective/Emergency LSCS
  • 3. Primary/Repeat LSCS
  • 4. With Pfannenstiel skin incision
  • 5. Under spinal anaesthesia with 2 ml of 0.5% bupivacaine (hyperbaric) and 25mcg fentanyl

排除标准

  • 1. Vertical skin incision
  • 2. Epidural labour analgesia
  • 3. General anaesthesia
  • 4. Allergic/having contraindications to the drugs used in study
  • 5. Uncontrolled diabetes
  • 6. Suffering from neuropathic / chronic pain / migraine
  • 7. History of substance abuse (alcohol/ tobacco/drug)
  • 8. On regular analgesic treatment
  • 9. Unable to understand VAS/Likert scale

研究者

发起方
All indian institute of medical sciences

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