跳至主要内容
临床试验/NCT04405336
NCT04405336已完成不适用

Effect of Tab Block and Patient Controlled Analgesia in Cesarean Section

Aljazeera Hospital1 个研究点 分布在 1 个国家目标入组 140 人开始时间: 2020年5月28日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
140
试验地点
1
主要终点
The number of women who will feel less pain post CS

研究概览

简要总结

cesarean section rate become increasing nowadays

详细描述

indication of cesarean section are different from case to case and the use of pain controlling agents is very important to relieve post operative pain

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 42 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • women coming for an elective CS

排除标准

  • women who has a n emergency CS or complicated normal deivery needs urgent CS

研究组 & 干预措施

giving tab block

Active Comparator

giving patients tab block

干预措施: tab block (Drug)

giving tab block

Active Comparator

giving patients tab block

干预措施: women who will not receive tab block or PCA (Drug)

giving PCA

Active Comparator

Giving PCA to patients

干预措施: PCA (Drug)

giving PCA

Active Comparator

Giving PCA to patients

干预措施: women who will not receive tab block or PCA (Drug)

结局指标

主要结局

The number of women who will feel less pain post CS

时间窗: 2 days

the degree of pain that will be felt post CS

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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Tab Block and Patient Controlled Analgesia in CS | 临床试验