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临床试验/NCT00097110
NCT00097110已完成3 期

RCT of Antioxidant Therapy to Prevent Preeclampsia in Brazil

NICHD Global Network for Women's and Children's Health1 个研究点 分布在 1 个国家目标入组 734 人开始时间: 2003年7月1日最近更新:
适应症
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
734
试验地点
1
主要终点
Incidence of preeclampsia

研究概览

简要总结

The perinatal morbidity and mortality rates for Brazil are five to ten-fold higher than those reported for upper income countries. This study tests the likelihood that the joint administration of antioxidants vitamin C (1000 mg) and vitamin E (400 IU) will reduce the incidence of preeclampsia among chronically hypertensive pregnant patients and patients with a past history of preeclampsia/eclampsia.

详细描述

The maternal, perinatal and neonatal morbidity and mortality rates for Brazil are five to ten-fold higher than those reported for upper income countries. In Sao Paulo, 22 percent of maternal deaths are attributable to hypertensive complications of pregnancy, which ranks as the number one cause of maternal death. Recent advances in the understanding of the pathophysiology of preeclampsia suggest the possibility of antioxidant therapy for the prevention of preeclampsia. The primary hypothesis is that the joint administration of the antioxidants vitamin C (1000 mg) and vitamin E (400 IU) will reduce the incidence of preeclampsia among chronically hypertensive pregnant patients and patients with a past history of preeclampsia/eclampsia. Secondary outcomes include severity of preeclampsia; incidence of gestational hypertension; incidence of premature rupture of the membranes; incidence of preterm birth; incidence of low birth weight infants; biomarker level correlation with preeclampsia.

Study sites are high-risk obstetrical clinics in the Brazilian cities of Recife, Botucatu, Campinas, and Porto Alegre. The sample size was based on an estimated risk of preeclampsia/eclampsia of 21-25% in the control group. The study hypothesizes a 40% absolute reduction of risk of preeclampsia; early treatment withdrawal of 3%; withdrawal of consent or loss to follow-up of 10%; calculated at a 0.05 significance level with 80% power. Seven hundred thirty-four obstetric patients with chronic hypertension or preeclampsia in the prior pregnancy presenting for care between 12 weeks and 19 weeks', 6 days gestation will be randomized to a double-blinded placebo controlled trial to receive a daily dose of either vitamin E (400 International Units) and vitamin C (1000 mg) or placebo from the time of enrollment to delivery. The use of MEMS caps enables researchers to accurately track compliance.

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
Double

入排标准

性别
Female
接受健康志愿者

入选标准

  • Gestational age between 12 weeks and 19 weeks, 6 days, inclusive
  • Chronic hypertension
  • History of preeclampsia/eclampsia
  • Attendance at a participating hospital (Recife, Botucatu, Campinas and Porto Alegre, Brazil)

排除标准

  • Planned delivery elsewhere.
  • Multifetal gestation.
  • Allergy to vitamin C or vitamin E.
  • Requirement for aspirin or anticoagulant medication.
  • Proteinuria ≥ 2+ on dipstick urine test; or proteinuria = 1+ on dipstick and ≥ 300 mg/24 hours.
  • Pre-pregnancy diabetes mellitus.
  • Known fetal anomaly incompatible with life.
  • Prior participation in the study.
  • Unwillingness to take the study medication.

结局指标

主要结局

Incidence of preeclampsia

次要结局

  • Frequency of abruptio placentae
  • Severity of preeclampsia
  • Incidence of small for gestational age
  • Biomarker level correlation with preeclampsia
  • Incidence of gestational hypertension or preeclampsia
  • Incidence of preterm birth
  • Incidence of low birth weight infants

研究者

发起方
NICHD Global Network for Women's and Children's Health
申办方类型
Network
责任方
Sponsor

研究点 (1)

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