A study to compare postoperative analgesic efficacy of ropivacaine alone or in combination with dexamethasone for TAP Block in open cholecystectomy

Pt BDSharma PGIMS ROHTAK1 个研究点分布在 1 个国家目标入组 60 人开始时间: 2016年1月13日最近更新: 2017年9月8日

适应症

试验速览

阶段: 2 期
状态: 招募中
发起方
入组人数: 60
试验地点: 1
主要终点: twenty four hours Tramadol consumption

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

This study is a randomized, double blind, parallel group, trail comparing the postoperative analgesic efficacy of 18ml of 0.75% ropivacaine with 2ml of normal saline with 18 ml of o.75% ropivacaine with 2 ml of dexamethasone for TAP block in open cholecystectomy over 60 patients of ASA grade 1-3. The primary outcome will be 24 hr tramadol cosumption. The secondary outcome will be measure include VAS score, nausea score, sedation score and any side effect.

研究设计

研究类型: Observational

入排标准

年龄范围: 20.00 Year(s) 至 60.00 Year(s)（—）
性别: All

入选标准

•ASA Grade 1-3.

排除标准

•1.Contraindication to regional anaesthesia 2.History of local anaesthetic allergy 3.Psychiatric disorder 4.BMI>35kg/sq.m 5.Diabetes Mellitus 6.Chronic opioid use 7.Patient refusal.

结局指标

主要结局

twenty four hours Tramadol consumption

时间窗: postoperative twenty four hours

次要结局

Time to first request for analgesic, VAS Score,Nausea Score, Sedation Score, Any side effect(24 Hours)

研究者

发起方

Pt BDSharma PGIMS ROHTAK

申办方类型

Government medical college

研究点 (1)

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