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临床试验/CTRI/2016/07/007076
CTRI/2016/07/007076招募中3 期

: Safety and Efficacy of abbreviated (12 hr) Magnesium Sulfate (MgSO4) therapy) vs. traditional 24 hrs therapy after delivery in Severe Preeclampsia: a Randomized Clinical Trial

DirectorPGIMER Chandigarh0 个研究点目标入组 240 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
招募中
发起方
入组人数
240

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

  • Inclusion Criteria
  • 1.Women with severe-preeclampsia, diagnosed during ante partum, intrapartum, or postpartum, are eligible for inclusion after delivery.
  • A diagnostic criterion for severe preeclampsia includes:
  • sustained systolic blood pressure of >=160 mm Hg;
  • sustained diastolic blood pressure of >=110 mm Hg;
  • proteinuria >3 + on dipstick or >=5 g/24- hour urine collection;
  • oliguria (urine output <500 mL in 24 hours );
  • the presence of persistent headache, visual disturbances, or epigastric or right upper quadrant pain; thrombocytopenia ; impaired liver function; pulmonary edema or cyanosis;
  • fetal growth retardation;
  • or superimposed severe pre-eclampsia with pre-existing chronic hypertension.
  • 2.Agree to comply with study procedures;
  • 3. > 18 years of age;
  • 4.Give informed consent for study participation

排除标准

  • Exclusion Criteria
  • Associated maternal diseases;
  • Use of illicit drugs or other medications that might interfere with maternal hemodynamics;
  • Contraindications to the use of magnesium sulfate: drug hypersensitivity, oliguria with urine output below 25ml/h; anuria (absent urine output), myasthenia gravis.
  • Comatosed patients
  • Pulmonary oedema
  • Patients who have received MgSO4, Phenytoin, Diazepam before coming to hospital
  • Intra cranial bleeding

研究者

发起方
DirectorPGIMER Chandigarh

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