CTRI/2024/05/067500尚未招募4 期
Evaluating the Efficacy and Timing of Tranexamic Acid Administration in Reducing Bleeding During and After Elective Lower Segment Cesarean Sections: A Randomized Double-Blind Placebo-Controlled Trial - NI
All India Institute of Medical Sciences Bibinagar0 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
- •All antenatal women = 18 years of age with singleton pregnancy planned for elective LSCS at gestation = 34 weeks.
排除标准
- •1. Women undergoing vaginal delivery
- •2. History of coagulation or thrombotic disorders, 3. Emergency LSCS,
- •4. Abruption or placenta praevia,
- •5. Abnormally invasive placenta,
- •6. Multifetal gestation,
- •7. Preeclampsia or HELLP syndrome,
- •8. Eclampsia,
- •9. Intrauterine fetal demise,
- •10. Polyhydramnios,
- •11. History of epilepsy or seizure,
- •12. Anticoagulant drugs or LMW Heparin,
- •13. Anemia/cardiac/renal/liver disease,
- •14. Hypersensitivity to TXA,
- •15. CS being done under General anesthesia.
研究者
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