跳至主要内容
临床试验/CTRI/2025/03/082720
CTRI/2025/03/082720尚未招募不适用

A Comparative Study Between Intrathecal Ropivacaine Alone Versus Synergistic Effect Of Intrathecal Fentanyl And Ropivacaine In Spinal Anaesthesia For Caesarean Section

Dr Prachi1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2025年4月28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
100
试验地点
1
主要终点
Hyperbaric ropivacaine 0.75% with Fentanyl in Spinal Anesthesia Caesarean Section found to have longer duration of sensory and motor blockage then hyperbaric ropivacaine 0.75% alone

研究概览

简要总结

The aim of the study is to compare and determine the effects of intrathecally administered 0.75% hyperbaric ropivacaine alone and 0.75% hyperbaric ropivacaine with fentanyl (25mcg) on reduction of higher blocks incidence simultaneously assess the onset, duration of sensory and motor block, quality of subarachnoid block, hemodynamic stability, perioperative analgesia and any adverse drug reactions in patients undergoing caesarean section.

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

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

入选标准

  • 1.Pregnant women scheduled for cesarean section 2.American Society of Anesthesiologists (ASA) physical status I or II.

排除标准

  • 1.Patients with contraindications to spinal anesthesia or opioids 2.ASA physical status III or higher 3.Patients with a history of opioid dependence or chronic pain syndromes.

结局指标

主要结局

Hyperbaric ropivacaine 0.75% with Fentanyl in Spinal Anesthesia Caesarean Section found to have longer duration of sensory and motor blockage then hyperbaric ropivacaine 0.75% alone

时间窗: Primary outcome assessed in 5 minutes

次要结局

  • Quality of subarachnoid block, hemodynamic(stability,perioperative analgesia in patients undergoing Caesarean Section are better in patients receiving ropivacine 0.75%)

研究者

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

Dr Prachi

Varun Arjun Medical College and Rohilkhand Hospital

研究点 (1)

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