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临床试验/CTRI/2017/06/008915
CTRI/2017/06/008915尚未招募4 期

A comparison of efficacy of prophylactic infusion of Phenylephrine versus Norepinephrine for the prevention of post spinal hypotension in parturients undergoing elective caesarean section- A randomized controlled trial

ALL INDIA INSTITUTE OF MEDICAL SCIENCES0 个研究点目标入组 130 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
入组人数
130

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 OF SINGLETON PREGNANCY WITH GESTATIONAL AGE OF MORE THAN 36 WEEKS OF GESTATION
  • 2. ASA I AND II WOME

排除标准

  • 1. Patient refusal
  • 2. Multiple gestation
  • 3. Pregnancy with severe systemic illness (uncontrolled diabetes, hypertension, cardiac disease, etc.)
  • 4. BMI > 40 kg/m2
  • 5. In active labour
  • 6. Suspected obstetric complications ( like polyhydraminos, IUGR)
  • 7. Patients in whom spinal anaesthesia is contraindicated (spinal abnormalities, infection at the site of injection, coagulopathies, raised intracranial tension)

研究者

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