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临床试验/NCT02396030
NCT02396030终止4 期

Effectiveness and Safety of 1g/Hour vs. 2g/Hour of Magnesium Sulfate Maintenance Dose for Eclampsia Prevention: Randomized Clinical Trial

Instituto Materno Infantil Prof. Fernando Figueira1 个研究点 分布在 1 个国家目标入组 62 人开始时间: 2015年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
终止
发起方
入组人数
62
试验地点
1
主要终点
ECLAMPSIA

研究概览

简要总结

Eclampsia is an obstetric emergency capable of prophylaxis. To prevent and control seizures, there is no doubt that the magnesium sulfate (MgSO4) is the ideal drug. However, there are still questions regarding its use and dose. The scheme and the optimal time of administration remain to be elucidated. The objective of this trial is to compare the effectiveness and safety of intravenous magnesium sulfate in the maintenance phase 1g / h versus 2 g / h to prevent eclampsia in pregnant and postpartum women with severe preeclampsia (pure or superimposed).

详细描述

Hypertensive disorders are frequent during the course of pregnancy-puerperal cycle and an important cause of maternal morbidity and mortality, fetal and perinatal. The high frequency of maternal death can be explained by the presence of numerous complications such as eclampsia. Eclampsia is an obstetric emergency capable of prophylaxis. To prevent and control seizures, there is no doubt that the magnesium sulfate (MgSO4) is the ideal drug. However, there are still questions regarding its use and dose. The scheme and the optimal time of administration remain to be elucidated. Currently, allows the use of either 1 g / h to 2 g / h of magnesium sulphate during the maintenance phase to prevent eclamptic convulsions. However, there is no report in the literature of randomized controlled trials comparing different doses of magnesium sulfate in the maintenance phase to prevent eclampsia.

The objective of this study is to compare the effectiveness and safety of intravenous magnesium sulfate in the maintenance phase 1g / h versus 2 g / h to prevent eclampsia in pregnant and postpartum women with severe preeclampsia (pure or superimposed).There will be a trial randomized and triple blind in the Integrative Medicine Institute Prof. Fernando Figueira (IMIP) from March 2015 to April 2017, and will be included 2000 women randomized into two groups: MgSO4 maintenance dose of 1 g / h or 2 g / h. Patients who had eclampsia before loading dose, with use of other medications or illicit drugs that may interfere with maternal hemodynamics or with contraindications to the use of magnesium sulfate will be excluded. The primary endpoint will be the incidence of eclampsia. Other complications such as oliguria, bleeding, recurrence of seizures, disseminated intravascular coagulation, maternal death, presence of side effects related to the use of MgSO, neonatal outcome and other variables will be considered secondary outcomes. Randomization for preventive treatment of eclamptic seizures with MgSO4 1g / h or MgSO4 2g / h will be held according to a table of sequential numbers from one to 2000, using the letters A and B and not knowing its meaning. The analysis will be performed with the groups identified as A or B, breaking the secrecy only after the results obtained and prepared the tables, or by resolution of the External Monitoring Committee.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
14 Years 至 50 Years(Child, Adult)
性别
Female
接受健康志愿者

入选标准

  • Severe Preeclampsia (pure and superimposed)

排除标准

  • Eclampsia before administration of the loading dose of MgSO4 ;
  • Use of other medications or illicit drugs that may interfere with maternal hemodynamics;
  • Contraindications to the use of magnesium sulfate: known hypersensitivity to the drug, oliguria with urine output below 25 ml per hour or anuria (urine output absent) and myasthenia gravis.
  • Use of mechanical ventilation

研究组 & 干预措施

Magnesium sulfate 50% - 1g/h

Active Comparator

After loading dose of 6g of magnesium sulfate, patients will receive the maintenance dose of 1g/hour of intravenous magnesium sulfate, for 24 hours

干预措施: Magnesium sulfate 50% - 1g/h (Drug)

Magnesium sulfate 50% - 2g/h

Experimental

After loading dose of 6g of magnesium sulfate, patients will receive the maintenance dose of 2g/hour of intravenous magnesium sulfate, for 24 hours

干预措施: Magnesium sulfate 50% - 2g/h (Drug)

结局指标

主要结局

ECLAMPSIA

时间窗: From end of loading dose, until 24 hours after delivery

Seizures that occur after the loading dose, during magnesium sulfate, until 24 hours after the delivery of the baby

次要结局

  • RECURRENCE(From end of loading dose, until 24 hours after delivery)
  • additional anticonvulsant(From end of loading dose, until 24 hours after delivery)
  • DISCONTINUATION OF MAGNESIUM SULFATE(From end of loading dose, until 24 hours after delivery)
  • OLIGURIA(From end of loading dose, until 15 days after delivery)
  • Placental abruption(From end of loading dose, until delivery of the child)
  • postpartum hemorrhage(From end of loading dose, until 48 hours after delivery)
  • COMPLICATIONS(From end of loading dose, until 3 hours after delivery)
  • thromboembolic complications(From end of loading dose, until 15 days after delivery)
  • liver failure(From end of loading dose, until 15 days after delivery)
  • RENAL FAILURE(From end of loading dose, until 15 days after delivery)
  • Disseminated intravascular coagulation (DIC)(From end of loading dose, until 15 days after delivery)
  • acute pulmonary edema(From end of loading dose, until 15 days after delivery)
  • Maternal death(From end of loading dose, until 42 days after delivery)
  • Composite maternal morbidity(From end of loading dose, until 42 days after delivery)
  • SIDE EFFECTS(From end of loading dose, until 24 hours after delivery)
  • GLUCONATE USE(From end of loading dose, until 24 hours after delivery)
  • MAGNESIUM LEVELS(From end of loading dose, until 24 hours after delivery)
  • Hypertensive crises(From end of loading dose, until 24 hours after delivery)

研究者

发起方
Instituto Materno Infantil Prof. Fernando Figueira
申办方类型
Other
责任方
Principal Investigator
主要研究者

Leila Katz

MD PhD

Instituto Materno Infantil Prof. Fernando Figueira

研究点 (1)

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