CTRI/2024/07/070533尚未招募3 期
Comparative study of Oxytocin 10 IU IM V/s Oral Misoprostol 600 MCG in active management of third stage of labour - NI
I0 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
- 3 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
- •1. Women with gestational age more than 28 weeks and at low risk , undergoing vaginal delivery.
- •2. Patients having the ability and willingness to provide an informed consent.
排除标准
- •1. Hb under 8gm
- •2. Previous pregnancy associated with PPH.
- •3. Patient with traumatic PPH due to genital laceration.
- •4. Antepartum haemorrhage.
- •5. Multiple pregnancies.
- •6. Non-cephalic presentation.
- •7. Multipara, big baby, fibroid uterus, polyhydramnios
- •8. Previous LSCS
- •9. Hypertension, pre-eclampsia or pregnancy induced hypertension.
- •10. Intra uterine death.
- •11. Seizures, diabetes, renal anomalies, cardiac arrest or coagulation disorders.
- •12. Choriamnionitis
- •13. Polyhydraminos.
- •14. Epidural anaesthesia.
- •15. Bronchial asthma or respiratory disorders.
研究者
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