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临床试验/CTRI/2024/11/076936
CTRI/2024/11/076936尚未招募Phase 3 4

Comparative study of Dexamethasone and Midazolam as adjuvants to Ropivacaine in Transversus abdominis plane block on post operative analgesia after Laparoscopic lower abdominal surgeries

Department of Anesthesiology Sir Sunderlal Hospital Institute of Medical Sciences BHU1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年11月29日最近更新:

试验速览

阶段
Phase 3 4
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
1. Time duration when first rescue analgesia was needed

研究概览

简要总结

A double-blind prospective randomised comparative study will be conducted on 60 patients scheduled for laparoscopic lower abdominal surgeries. Patients will be randomly allocated using computer generated random number to be treated with either dexamethasone (Group D) or preservative free midazolam (Group M). After completion of surgery ultrasound guided TAP block will be performed in patients of both the groups. Patients in Group D will receive 0.2% ropivacaine (20 ml) and 2ml normal saline containing 4mg dexamethasone whereas patients in Group M will receive 0.2% ropivacaine (20 ml) and 2ml normal saline containing 2 mg of preservative free midazolam. Patients will be shifted to post anaesthesia care unit (PACU) where post-op monitoring of pain (by VAS score), sedation (by Ramsay sedation scale), postoperative nausea and/or vomiting (0: no nausea; 1: nausea no vomiting; and 2: nausea and vomiting), and complications (like pruritus, headache, local anaesthetic systemic toxicity) will be done till 24h after surgery

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
20.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • Patient undergoing Laparoscopic lower abdominal surgeries.
  • ASA 1 or 2 physical status.

排除标准

  • Refusal of consent.
  • Local site infection.
  • Any contraindication to peripheral nerve block.
  • Morbid obese (BMI more than or equal to 40kg/m2)
  • Dropout ( Laparoscopic surgeries converted into open surgeries).

结局指标

主要结局

1. Time duration when first rescue analgesia was needed

时间窗: Immediately after shifting to post-op, 1 Hour, 2 Hour, 4 Hour, 6 Hour, 8 Hour, 12 Hour, 16 Hour, 20 Hour, 24 Hour

2. Total dose of rescue analgesia

时间窗: Immediately after shifting to post-op, 1 Hour, 2 Hour, 4 Hour, 6 Hour, 8 Hour, 12 Hour, 16 Hour, 20 Hour, 24 Hour

次要结局

  • To study hemodynamic variability, post-op nausea and vomiting and sedation.(within 24 hours post operatively.)

研究者

发起方
Department of Anesthesiology Sir Sunderlal Hospital Institute of Medical Sciences BHU
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

vaibhav kumar

Institute of Medical Sciences, BHU

研究点 (1)

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