Antioxidant Supplementation in Pregnant Women With Low Antioxidant Status

NCT00388856 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 400

Last updated 2010-02-17

No results posted yet for this study

Summary

The purpose of this study is to investigate antioxidants supplementation in pregnant women with low antioxidant status at 10-12 weeks gestation age in relation to adverse pregnancy outcome in randomized prospective study.

Conditions

Interventions

DRUG

Vitamin C 1000mg and E 400IU

Sponsors & Collaborators

  • Indonesia University

    collaborator OTHER
  • Showa University

    lead OTHER

Principal Investigators

  • Akihiko Sekizawa, MD, PhD · Showa University School of Medicine

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
17 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2006-10-31
Primary Completion
2009-11-30
Completion
2010-02-28

Countries

  • Indonesia

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00388856 on ClinicalTrials.gov