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RCT of Antioxidant Therapy to Prevent Preeclampsia in Brazil

RCT of Antioxidant Therapy to Prevent Preeclampsia in Brazil

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00097110
Enrollment
734
Registered
2004-11-18
Start date
2003-07-31
Completion date
2006-12-31
Last updated
2013-11-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Eclampsia, HELLP Syndrome, Preeclampsia, Pregnancy

Keywords

Vitamin C, Vitamin E, Preeclampsia, Antioxidants, Global Network, Preterm birth, Low birth weight infants, Brazil, Brasil, Maternal and child health, International, Women's health

Brief summary

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.

Detailed description

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.

Interventions

Sponsors

Global Network for Women's and Children's Health Research
CollaboratorOTHER
Bill and Melinda Gates Foundation
CollaboratorOTHER
Fogarty International Center of the National Institute of Health
CollaboratorNIH
National Center for Complementary and Integrative Health (NCCIH)
CollaboratorNIH
National Institute of Dental and Craniofacial Research (NIDCR)
CollaboratorNIH
National Cancer Institute (NCI)
CollaboratorNIH
RTI International
CollaboratorOTHER
University of Cincinnati
CollaboratorOTHER
Universidade Federal de Pernambuco
CollaboratorOTHER
Feculdade de Medicina da Universidade de Sao Paulo - Brasil
CollaboratorOTHER
Faculdade de Medicina de Botucatu, UNESP, Botucatu, Brasil
CollaboratorOTHER
University of Campinas, Brazil
CollaboratorOTHER
Hospital de Clinicas de Porto Alegre
CollaboratorOTHER
NICHD Global Network for Women's and Children's Health
Lead SponsorNETWORK

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
Yes

Inclusion criteria

* 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)

Exclusion criteria

* 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.

Design outcomes

Primary

MeasureTime frame
Incidence of preeclampsia

Secondary

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

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 6, 2026