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
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