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临床试验/ISRCTN71886984
ISRCTN71886984已完成不适用

Prevention of oxytocin-induced hypotension in caesarean delivery by co-administration of phenylephrine with oxytocin: a prospective randomised double-blind controlled study

Ministry of Health (Brunei)0 个研究点目标入组 200 人开始时间: 2012年4月4日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
200

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

性别
Female

入选标准

  • 1. American Society of Anesthesiologists (ASA) class l and ll undergoing elective caesarean section
  • 2. Age between 18 to 35 years
  • 3. Body mass index (BMI) less than 35 kg/m2
  • 4. Spinal anaesthesia

排除标准

  • 1. Placenta previa
  • 2. Thrombocytopenia
  • 3. Coagulopathies
  • 4. Previous major obstetrics haemorrhage (more than 1000 ml)
  • 5. Known fibroid
  • 6. Receiving anticoagulant therapy
  • 7. Anemia (hemoglobin less than 9 g/dl)
  • 8. Body mass index greater than 35 kg/m2
  • 9. Preeclampsia
  • 10. Cardiac, respiratory and renal disease
  • 11. Known allergy to any protocol medicine

研究者

发起方
Ministry of Health (Brunei)

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