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临床试验/CTRI/2025/10/096332
CTRI/2025/10/096332尚未招募不适用

Incidence risk factors and pattern of distribution of pruritis in patients receiving intrathecal fentanyl as an adjuvant to spinal anaesthesia with hyperbaric bupivacaine

sparsh singhal1 个研究点 分布在 1 个国家目标入组 96 人开始时间: 2025年11月1日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
96
试验地点
1
主要终点
To estimate the incidence of pruritic with intrathecal fentanyl

研究概览

简要总结

In this study, patients undergoing surgery under spinal anaesthesia will receive intrathecal bupivacaine with fentanyl as additive as a part of standard protocol of our institution, and the occurrence of pruritus (itching) will be assessed., the procedure will be explained to the participant in detail and informed consent will be taken. No specific orders to be followed for the sake of our study as it is purely an observational study which does not involve any painful procedure. In the operation theatre just before surgery patients receiving spinal anaesthesia with bupivacaine with fentanyl will be assessed for severity of itching and site of itching

研究设计

研究类型
Observational

入排标准

年龄范围
18.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • ASA 1 and 2 patients undergoing surgeries under spinal anaesthesia.

排除标准

  • Patients with allergy to opioids preexisting pruritis; preeclampsia; diabetes mellitus.

结局指标

主要结局

To estimate the incidence of pruritic with intrathecal fentanyl

时间窗: during operative and one hour post operative duration

次要结局

  • to look for risk factors associated and pattern of distribution of pruritis with intrathecal fentanyl(during operative and one hour post operative duration)

研究者

发起方
sparsh singhal
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

sparsh singhal

kmc manipal

研究点 (1)

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