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临床试验/PACTR202208859856197
PACTR202208859856197尚未招募未知

Two Different Doses of Tranexamic Acid for reduction of Perioperative Blood Loss in Cesarean Section: a randomized controlled study

faculty of medicine suez canal university0 个研究点目标入组 134 人开始时间: 2022年8月5日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
入组人数
134

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

年龄范围
19 Year(s) 至 44 Year(s)(—)
性别
Female

入选标准

  • 1)Age from 18- 45 years.
  • 2)Patients are ASA I (American Society of Anesthesiology physical status Grade I) = (normal healthy patients) or ASA II (American Society of Anesthesiologists physical status Grade II) = (patients with mild systemic disease and no functional limitations).
  • 3)term with singleton uncomplicated pregnancies.
  • 4)Body mass index of at most 40 kg/m2.

排除标准

  • 1)Parturient with peri-partum disorders as DM, HTN, cardiac diseases, Sickle cell disease or bleeding disorders History of venous (deep vein thrombosis and/or pulmonary embolism) or arterial (angina pectoris, myocardial infarction, stroke) thrombosis.
  • 2)Known case of coagulation disorders.
  • 3)Severe anemia.
  • 4)Allergy to TXA.
  • 5)Severe medical and surgical complications involving the heart, liver, kidney, brain, and blood disorder.
  • 6)Abnormal placenta such as placenta previa and placental abruption.
  • 7)Pregnancy related complication like severe preeclampsia,
  • 8)Pregnancy with <37 weeks gestational age.
  • 9)Woman on anticoagulant therapy during the week
  • 10)Refusal to participate in the study

研究者

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