Impact of Prenatal Vitamin/Mineral Supplements on Perinatal Mortality

Sponsor
Centers for Disease Control and Prevention (U.S. Fed)
Overall Status
Completed
CT.gov ID
NCT00133744
Collaborator
(none)
18,962
5
3
55
3792.4
68.9

Study Details

Study Description

Brief Summary

The purpose of this study is to determine whether a daily prenatal supplement of iron plus folic acid or a daily prenatal supplement with multiple vitamins and minerals given to women from their first prenatal visit through delivery reduces perinatal mortality compared with a daily prenatal supplement of folic acid alone.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: folic acid
  • Dietary Supplement: folic acid plus iron
  • Dietary Supplement: supplements with multiple vitamins and minerals
Phase 3

Detailed Description

In the project area in China, the rate of perinatal mortality (stillbirths and infant deaths within 6 days of birth) is two times that of the United States. Causes of perinatal mortality include, but are not limited to, low birth weight and preterm delivery. Anemia (low hemoglobin) among pregnant women is associated with low birth weight and preterm delivery and also is elevated in the project area. Supplements of iron, folic acid, and other vitamins and minerals can prevent anemia among pregnant women, but the effects of these supplements on other maternal and infant health outcomes are unclear.

Since 1993, the People's Republic of China has recommended that newly married women, and those who plan pregnancy, take 400μg of folic acid daily through the first trimester of pregnancy. Although WHO recommends that pregnant women take iron and folic acid supplements, there is currently no national recommendation that pregnant women in China take iron or other vitamin or mineral supplements (other than folic acid). UNICEF is now testing a prenatal vitamin and mineral supplement in programs to prevent low birth weight. Our study will provide additional information about the health impact of the UNICEF prenatal supplement versus an iron and folic acid supplement versus folic acid alone.

Comparisons:
  • Infants of women who receive daily prenatal supplements that contain 400μg folic acid alone, will be compared with infants of women who receive daily supplements that contain 30 mg iron and 400 μg folic acid.

  • Infants of women who receive daily supplements that contain 30 mg iron and 400 μg folic acid will be compared with infants of women who receive a daily supplement containing 30 mg iron, 400μg folic acid and other vitamins and minerals (UNICEF formulation).

Study Design

Study Type:
Interventional
Actual Enrollment :
18962 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Impact of Iron/Folic Acid Versus Multimicronutrient Versus Folic Acid Supplements During Pregnancy on Mortality, Morbidity, and Complications During Pregnancy, Labor, and Delivery: A Randomized Controlled Trial in China
Study Start Date :
May 1, 2006
Actual Primary Completion Date :
Dec 1, 2009
Actual Study Completion Date :
Dec 1, 2010

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: A, 1

Dietary Supplement: folic acid
pills by mouth, one per day, from the first prenatal visit until delivery, 400 micrograms (mcg) folic acid

Experimental: A, 2

Dietary Supplement: folic acid plus iron
pills by mouth, one per day, from the first prenatal visit until delivery, 400 mcg folic acid, 30 mg Fe

Experimental: A, 3

Multiple micronutrient supplement

Dietary Supplement: supplements with multiple vitamins and minerals
pills, one per day, from the first prenatal visit until delivery; folic acid 400 mcg, Fe 30 mg, vitamin(vit) A 800 mcg, vit E 10 mg, vit D 5 mcg, vit C 70 mg, vit B1 1.4 mg, vit B2 1.4 mg, vit B6 1.9 mg, vit B12 2.6 mcg, Niacin 18 mg, Zn 15 mg, Cu 2mg, Iodine 150 mcg, Selenium 65 mcg
Other Names:
  • UNIMMAP
  • Outcome Measures

    Primary Outcome Measures

    1. Perinatal mortality, i.e., the number of stillbirths (fetal deaths of 28 weeks or more of gestation) and the number of deaths within the first 0-6 days of life per 1000 births (live births and stillbirths) [20 weeks gestation to 6 days postpartum]

    Secondary Outcome Measures

    1. Maternal anemia [24-28 weeks gestation]

    2. Maternal anemia [4-8 weeks postpartum]

    3. Infant gestational age at birth, preterm delivery [delivery]

    4. Infant birth weight, low birth weight [at birth]

    5. Infant low weight-for-height [infant age 6 months and 12 months]

    6. Infant anemia [6 months and 12 months of age]

    7. maternal gastrointestinal side effects [monthly from a month after enrollment until delivery]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    20 Years and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Live in one of the study counties (Laoting, Mancheng, Fengrun, Xianghe, Yuanshi)

    • Can follow instructions

    • Can swallow pills

    Exclusion Criteria:
    • = 20 weeks gestation at enrollment

    • Previous live birth

    • Anemic (hemoglobin [Hb] <10 g/dl in 1st trimester and < 9.5 g/dl in 2nd trimester) at enrollment

    • Current use of iron or other vitamin or mineral supplements (except folic acid)

    • Age < 20 years at enrollment

    • Under treatment for anemia at enrollment

    • Refuse to participate

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Fengrun Maternal and Child Health Institute Fengrun Hebei China 064000
    2 Laoting Maternal and Child Health Institute Laoting Hebei China 063600
    3 Mancheng Maternal and Child Health Institute Mancheng Hebei China 072150
    4 Xianghe Maternal and Child Health Institute Xianghe Hebei China 065400
    5 Yuanshi Maternal and Child Health Institute Yuanshi Hebei China 051130

    Sponsors and Collaborators

    • Centers for Disease Control and Prevention

    Investigators

    • Principal Investigator: Weicheng You, MD, MBA, Peking University Health Science Center, Beijing China
    • Study Director: Jianmeng Liu, MD, PhD, Institute of Reproductive and Child Health, Peking University Health Science Center, Beijing China

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00133744
    Other Study ID Numbers:
    • CDC-NCCDPHP-4084
    First Posted:
    Aug 24, 2005
    Last Update Posted:
    Mar 21, 2011
    Last Verified:
    Mar 1, 2011

    Study Results

    No Results Posted as of Mar 21, 2011