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临床试验/CTRI/2012/12/003258
CTRI/2012/12/003258已完成Unknown

Comparison of postoperative analgesic effect of clonidine through intravenous administration versus wound infiltration in patients undergoing open cholecystectomy

Director1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2009年9月9日最近更新:
适应症

试验速览

阶段
Unknown
状态
已完成
发起方
入组人数
60
试验地点
1
主要终点
Postoperative pain and analgesic requirement

研究概览

简要总结

This randomized double- blind study was conducted to compare the postoperative analgesic effect of clonidine when administered intravenously or in wound infiltration with bupivacaine. 60 adult patients of ASA grade I-II undergoing elective open cholecystectomy were randomly allocated into three groups. Group 1 (control group) patients received wound infiltration with 30 ml 0.25% bupivacaine at the end of surgery. Group 2 patients received 3 mcg/kg clonidine IV plus wound infiltration with bupivacaine, while group 3 patients received 3 mcg/kg clonidine in would infiltration with bupivacaine. Postoperative analgesia was provided with intravenous diclofenac 8 hourly and morphine on demand. The postoperative pain, number of patients requiring rescue analgesia and total morphine consumption during 24 postoperative hours was recorded. Patients were observed for any adverse effects like excessive sedation, nausea-vomiting, hypotension and bradycardia.

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 60.00 Year(s)(—)
性别
All

入选标准

  • •Patients posted for elective open cholecystectomy under general anesthesia.

排除标准

  • •Patients with ASA physical status 3 or 4, Patients with morbid obesity, patients receiving adrenoceptor agonist, antagonist or narcotics.

结局指标

主要结局

Postoperative pain and analgesic requirement

时间窗: 24 postoperative hours

次要结局

  • Side effects, like sedation, nausea-vomiting, hypotension and bradycardia(Patients satisfaction score)

研究者

发起方
Director
申办方类型
Research institution and hospital

研究点 (1)

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