Clinical Trials Directory

Trials / Completed

CompletedNCT00953134

Periconceptional Iron Supplementation in Rural Bangladesh

Periconceptional Iron Supplementation on Iron and Folate Indicators Among Pregnant and Non-pregnant Women in Rural Bangladesh.

Status
Completed
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
273 (actual)
Sponsor
The Hospital for Sick Children · Academic / Other
Sex
Female
Age
40 Years
Healthy volunteers
Accepted

Summary

The investigators hypothesize that periconceptional iron supplementation to married, nulliparous women in rural Bangladesh will significantly reduce anemia and improve hemoglobin concentrations before and during pregnancy.

Detailed description

In 2007, the National Strategy for Anemia Prevention and Control in Bangladesh included adolescents and newly married women as target groups for future iron and folic acid (IFA) supplementation programs. This double-blinded RCT examined the effect of daily periconceptional IFA vs. folic acid (FA) on anemia and iron indictors before and during pregnancy among married, nulliparous women in rural Bangladesh. Biochemical indices were collected at baseline and either at 15 weeks gestation or after 9 months among non-pregnant women (NPW).

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTFerrous fumarate (iron)60 mg of ferrous fumarate
DIETARY_SUPPLEMENTfolic acid400 mcg folic acid

Timeline

Start date
2007-02-01
Primary completion
2008-02-01
Completion
2008-03-01
First posted
2009-08-06
Last updated
2021-04-19

Locations

1 site across 1 country: Bangladesh

Source: ClinicalTrials.gov record NCT00953134. Inclusion in this directory is not an endorsement.