跳至主要内容
临床试验/CTRI/2022/11/047103
CTRI/2022/11/047103尚未招募不适用

A prospective randomized double blind control study comparing the analgesic efficacy of intraperitoneal Ropivacaine with Dexmedetomidine and Ropivacaine with Clonidine in patients undergoing elective laparoscopic cholecystectomy

Department of Anesthesiology1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2022年11月21日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
90
试验地点
1
主要终点
Numerical Rating Score (NRS)

研究概览

简要总结

This study is a prospective randomized double-blind control study comparing the analgesic efficacy of Ropivacaine with a2 agonist adjuvants for intraperitoneal instillation in patients undergoing laparoscopic cholecystectomy in KR 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
19.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • All ASA grade I and grade II patients between 19-60 years age group.

排除标准

  • ·All ASA grade III and IV patients.
  • ·Diabetes and Hypertension.
  • ·Cardiovascular, respiratory and neurological disorders.
  • ·Obesity (BMI>30kg/m2).
  • ·Drug allergy.

结局指标

主要结局

Numerical Rating Score (NRS)

时间窗: 24 hours

Time for first request of analgesia

时间窗: 24 hours

次要结局

  • Adverse effects(24 hours)
  • Patient satisfaction(48 hours)

研究者

申办方类型
Government medical college

研究点 (1)

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