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临床试验/CTRI/2018/06/014619
CTRI/2018/06/014619已完成不适用

Peritubal infiltration of fentanyl versus dexmedetomidine with ropivacaine in percutaneous nephrolithotomy; a prospective randomized comparative study

sumit soni1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2018年6月7日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
60
试验地点
1
主要终点
VAS score and DVAS score

研究概览

简要总结

this study is a randomised double blind, comparing analgesic efficasy of dexmedetomidine and fentanyl used as an adjuvant to ropivacaine in peritubal tract block in percutaneous nephrolithotomy that will be conducted in a tertiary care hospital in north india. the primary outcome measure will be VAS score and DVAS score  in the two groups and total rescue analgesic requirement within 48 hrs in post-operative period.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant and Outcome Assessor 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

  • adult , ASA grade 1 and ASA grade 2.

排除标准

  • patients requiring supracostal puncture or more than one puncture, patients having excessive intraoperative bleeding, stone size more than 3 cm.

结局指标

主要结局

VAS score and DVAS score

时间窗: VAS score and DVAS score assessed at 0 hrs, every hour for next 2 hours, every 2 hour for next 4 hours, and every 6 hour till 48 hours

次要结局

  • total rescue analgesic requirement(48 hrs)

研究者

发起方
sumit soni
申办方类型
Other [investigator iniated trial]

研究点 (1)

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