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临床试验/CTRI/2024/02/062430
CTRI/2024/02/062430尚未招募4 期

A Quasi experimental study to compare the efficacy of Carbetocin and Oxytocin in preventing post partum hemorrhage during vaginal delivery in a tertiary care center in Chengalpattu district

Dr Monisha S1 个研究点 分布在 1 个国家目标入组 62 人开始时间: 2024年2月15日最近更新:
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试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
62
试验地点
1
主要终点
To compare the efficacy of carbetocin with oxytocin in control of post partum hemorrhage
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

A QUASI EXPERIMENTAL STUDY TO COMPARE THE EFFICACY OF CARBETOCIN VS OXYTOCIN IN PREVENTING POST PARTUM HEMORRHAGE DURING VAGINAL DELIVERY IN A TERTIARY CARE CENTER IN CHENGALPATTU DISTRICT

PRIMARY OBJECTIVE:TO ASSESS THE EFFICACY OF CARBETOCIN AND TO COMPARE IT WITH OXYTOCIN IN CONTROL OF POST PARTUM HEMORRHAGE

SECONDARY OBJECTIVE:

TO STUDY THE SAFETY OF CARBETOCIN AND OXYTOCIN FOR USE IN

PREVENTION OF POST PARTUM HEMORRHAGE.

TO STUDY THE ADDITIONAL NEED OF UTEROTONIC AGENT FOLLOWING

CARBETOCIN AND OXYTOCIN ADMINISTRATION.

研究设计

研究类型
Interventional
分配方式
Other
盲法
None

入排标准

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

入选标准

  • •SINGLETON PREGNANCY TERM(37 TO 40 WEEKS OF GESTATION) VAGINAL DELIVERY.

排除标准

  • •AGE ABOVE 35 YEARS PREVIOUS LOWER SEGMENT CAESAREAN SECTION INSTRUMENTAL VAGINAL DELIVERY INCLUDING FORCEPS OR VACUUM ASSISTED COMPLETE PERINEAL TEAR DURING NORMAL VAGINAL DELIVERY HIGH RISK PREGNANCIES INCLUDING ANTEPARTUM HEMORRHAGE PLACENTA PREVIA ABRUPTIO PLACENTA PIH PRE ECAMPSIA ECLAMPSIA GDM MULTIPLE PREGNANCIES POLYHYDRAMNIOS MACROSOMIA.

结局指标

主要结局

To compare the efficacy of carbetocin with oxytocin in control of post partum hemorrhage

时间窗: 2 hours

次要结局

  • To study the safety & the additional need of uterotonic agent following carbetocin & oxytocin administration in prevention of post partum hemorrhage in 24 hours(24 hours)

研究者

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

DrMonisha S

Shri Sathya Sai Medical College and Research institute

研究点 (1)

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