PACTR202304555642144尚未招募3 期
The Effectiveness and Safety of 12-hour Versus 24-hour Magnesium Sulfate Regimen for the Management of Severe Preeclampsia in Sudanese Women: An Open Randomized Controlled Clinical Trial.
Samah Mohammed Ahmed Hussein0 个研究点目标入组 320 人开始时间: 2023年2月2日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 320
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
- 年龄范围
- 19 Year(s) 至 44 Year(s)(—)
- 性别
- Female
入选标准
- •Pregnant women with a viable fetus.
- •Age from 18 to 44 years old.
- •Admitted to the hospital's obstetrics unit for inpatient care.
- •Diagnosed with severe preeclampsia.
- •Severe preeclampsia is defined as blood pressure equal to or greater than 160/110 mm Hg at a single reading with proteinuria of 2+ on dipstick or 24-hour urinary protein of more than 5g, oliguria urine output of less than less than 30 mL/hour, cerebral or visual disturbances, renal failure as persistent oliguria despite of using of intravenous fluid and furosemide challenge with deranged serum electrolytes, rising creatinine greater than 1.5 mg/L, and urea greater than 45 mg/ dL”, pulmonary edema or cyanosis, epigastric or right upper quadrant pain, impaired liver function, thrombocytopenia, or fetal growth restriction.
排除标准
- •Women with any condition considered as a contraindication for MgSo4 therapy, like:
- •Drug hypersensitivity
- •Myasthenia gravis
- •Prior intake of any other anticonvulsant
- •History of epilepsy
- •Women with diabetes mellitus.
- •Women with HELP syndrome (hemolysis, elevated liver enzymes, and low platelets).
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