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临床试验/CTRI/2012/04/002553
CTRI/2012/04/002553已完成未知

Randomized Controlled Trial Comparing Two Different Regimes of Magnesium Sulphate in Severe Pre-eclampsia: A Pilot Study - PIPES Trial

JIPMER0 个研究点目标入组 402 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
JIPMER
入组人数
402

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

  • Any pregnant woman with Severe Pre- eclampsia as per the ACOG Criteria:
  • oSystolic blood pressure of 160 mm Hg or higher or diastolic blood pressure of 110 mm Hg or higher on two occasions at least 6 hours apart.
  • oProteinuria of 5 gm or higher in a 24-hour urine specimen or 3+ or greater on two random urine samples collected at least 4 hours apart.
  • oOliguria of less than 500 ml in 24 hours.
  • oCerebral or visual disturbances
  • oPulmonary edema or cyanosis
  • oEpigastric or right upper-quadrant pain
  • oImpaired liver function
  • oThrombocytopenia
  • oFetal growth restriction

排除标准

  • oMultiple Pregnancy
  • oPlatelet count < 50,000/mm3
  • oPlasma creatinine value >= 2mg/dl
  • oComatose patients
  • oDeranged coagulation profile
  • oKnown case of myasthenia gravis
  • oKnown case of seizure disorder
  • oPatients with Eclampsia (defined as presence of new-onset grand mal seizures in a woman with preeclampsia).
  • oHypersensitivity to Magnesium.
  • oWomen who have received have received magnesium sulphate therapy before being referred.

研究者

发起方
JIPMER

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