跳至主要内容
临床试验/CTRI/2024/04/065748
CTRI/2024/04/065748尚未招募4 期

Carbetocin and oxytocin in elective cesarean delivery in patients with high risk of postpartum hemorrhage under spinal anesthesia a comparative double blind randomized control study - NI

Tezpur medical college and hospital0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • Parturients of the ASA grade 1 and 2 with gestation of 37 weeks or more, who had an elective cesarean delivery under spinal anesthesia with risk factors of postpartum haemorrhage such as multiple pregnancy,two or more previous cesarean section,presence of uterine fibroids,previous myomectomy,past history of postpartum haemprrhage,prolonged labor,fetal macrosomia,BMI 35 and more and fetal malformations with polyhydramnios

排除标准

  • ASA garde 2, allergy to study drugs,patients contraindicated for spinal anesthesia,Declined to participate,premature rupture of memebrane,pregnancy induced hypertension,antepartum haemorrhage,patients in active labor,inadequate block after apinal anaesthesia,history of epilepsy,diabetes mellitus,ischemic heart disease,cerebrovascular disease,hepatic and renal disease

研究者

发起方
Tezpur medical college and hospital

相似试验

Comparing injection carbetocin and oxytocin in... | 临床试验