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临床试验/PACTR202304555642144
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).

研究者

发起方
Samah Mohammed Ahmed Hussein

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