跳至主要内容
临床试验/CTRI/2024/06/068438
CTRI/2024/06/068438尚未招募不适用

A comparative study on the effect of intravenous dexamethasone vs placebo in subarachnoid block with 0.5 percent hyperbaric bupivacaine for elective cesarean section

Gauhati Medical College and Hospital1 个研究点 分布在 1 个国家目标入组 74 人开始时间: 2024年7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
74
试验地点
1
主要终点
To evaluate the duration of analgesia when intravenous dexamethasone is added in patients receiving spinal anesthesia with 0.5% hyperbaric bupivacaine.

研究概览

简要总结

WE CAN EVALUATE THE DURATION OF ANALGESIA WHEN IV DEXAMETHASONE GIVEN WITH SPINAL ANESTHESIA.WE CAN ALSO EVALUATE THE DURATION OF SENSORY AND MOTOR BLOCK IF IV DEXAMETHASONE IS ADDED.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Double

入排标准

年龄范围
18.00 Year(s) 至 35.00 Year(s)(—)
性别
Female

入选标准

  • 1.Pregnant women between the age 18years to 35 years.
  • 2.All the cases should be elective LSCS cases.

排除标准

  • 1.Patients not giving consent.
  • 2.Patients having coagulopathy.

结局指标

主要结局

To evaluate the duration of analgesia when intravenous dexamethasone is added in patients receiving spinal anesthesia with 0.5% hyperbaric bupivacaine.

时间窗: 2,4,6,12,24 POSTOPERATIVE HOURS

次要结局

  • to evaluate the duration of motor and sensory block when iv dexamethasone is added in spinal anesthesia in LSCS.(2,4,6,12,24 POSTOPERATIVE HOURS)

研究者

发起方
Gauhati Medical College and Hospital
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Isita Jana

Gauhati Medical College And Hospital

研究点 (1)

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