临床试验/CTRI/2024/04/065815

CTRI/2024/04/065815尚未招募2/3 期

A comparative study between Oxytocin and Carbetocin for the prevention of primary postpartum hemorrhage following caesarean delivery.

self1 个研究点分布在 1 个国家目标入组 100 人开始时间: 2024年4月26日最近更新: 2024年4月15日

试验速览

阶段: 2/3 期
状态: 尚未招募
发起方
入组人数: 100
试验地点: 1
主要终点: Evaluation of hemodynamic effects of carbetocin in terms of blood loss.

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

This study is randomised parallel group controlled trial comparing the efficacy of oxytocin and carbetocin for the prevention of primary postpartum hemorrhage following ceserean delivery done in 100 pregnant women in North bengal medical college and hospital,darjeeling. The primary outcome evaluates the hemodynamic effects of carbetocin in terms of blood loss .The secondary outcome evaluates the need of additional uterotonics ,blood transfusion and adverse effects encountered by participants.

研究设计

研究类型: Interventional
分配方式: Randomized
盲法: None

入排标准

年龄范围: 18.00 Year(s) 至 40.00 Year(s)（—）
性别: Female

入选标准

•female with singleton, fullterm pregnancy undergoing elective or emergency caesarean section,.

排除标准

•Hypersensitivity to study drugs, Cases of coagulopathy,uterine fibroid,suspected placental pathology, Medical diseases such as hypertension,diabetes mellitus,Cardiac ,renal,liver disorders .

结局指标

主要结局

Evaluation of hemodynamic effects of carbetocin in terms of blood loss.

时间窗: 24 hours after ceserean section

次要结局

1.Need of additional uterotonics(2.Need of blood transfusion to compensate the blood loss.)

研究者

发起方

self

申办方类型

Other [other]

责任方

Principal Investigator

主要研究者

Adhi lakshmi

North Bengal Medical College and Hospital

研究点 (1)

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