临床试验/CTRI/2020/10/028697

CTRI/2020/10/028697尚未招募不适用

Evaluation of propofol sparing effect of intravenous lignocaine in patients undergoing daycare upper G.I. endoscopic procedures

Indira Gandhi Institute of Medical Sciences1 个研究点分布在 1 个国家目标入组 90 人开始时间: 2020年10月30日最近更新: 2020年10月28日

试验速览

阶段: 不适用
状态: 尚未招募
发起方: Indira Gandhi Institute of Medical Sciences
入组人数: 90
试验地点: 1
主要终点: 1.Total amount of propofol administered during the procedure

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

Sedation protocol employed during endoscopic procedures might hinder early recovery and discharge from hospital.We intend to observe whether addition of lignocaine to sedation protocol help early discharge from hospital.

研究设计

研究类型: Interventional
分配方式: Computer generated randomization
盲法: Participant and Investigator Blinded

入排标准

年龄范围: 18.00 Year(s) 至 65.00 Year(s)（—）
性别: All

入选标准

•Patients of age 18-65 years ASA Grade-I & II Undergoing day care upper G.I. endoscopic procedures under sedation.

排除标准

•Patient refusal ASA Grade-III & IV Unstable hemodynamic status Mental disorders, such as schizophrenia and psychosis on long-term psychotropic drugs Hyperalgesia or refractory cancer pain Allergic to study agent.

结局指标

主要结局

1.Total amount of propofol administered during the procedure

时间窗: After procedure

2.Total supplemental amount of propofol after induction and

时间窗: After procedure

3.Number of boluses of supplemental propofol

时间窗: After procedure

次要结局

Recovery scores(VAS score)

研究者

发起方

Indira Gandhi Institute of Medical Sciences

申办方类型

Government medical college

研究点 (1)

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