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| Sponsor: | Johns Hopkins Bloomberg School of Public Health |
|---|---|
| Collaborators: |
United States Agency for International Development (USAID) Bill and Melinda Gates Foundation The Canadian International Development Agency The Sight and Life Research Institute Access Business Group |
| Information provided by: | Johns Hopkins Bloomberg School of Public Health |
| ClinicalTrials.gov Identifier: | NCT00198822 |
Purpose
The purpose of this trial is to determine whether providing women with a weekly oral supplement of vitamin A, either preformed or as beta-carotene, at a dosage equivalent to a recommended intake from early pregnancy through three months postpartum, can reduce the risk of maternal mortality, fetal loss, or infant mortality.
| Condition | Intervention | Phase |
|---|---|---|
|
Vitamin A Deficiency |
Drug: Vitamin A or Beta-Carotene Supplements |
Phase III |
| Study Type: | Interventional |
| Study Design: | Prevention, Randomized, Double-Blind, Placebo Control, Single Group Assignment, Efficacy Study |
| Official Title: | Impact of Maternal Vitamin A or Beta-Carotene Supplementation on Maternal and Infant Mortality in Bangladesh |
| Estimated Enrollment: | 68000 |
| Study Start Date: | August 2001 |
| Estimated Study Completion Date: | May 2007 |
Maternal mortality and vitamin A deficiency coexist in rural South Asia. In Nepal, weekly supplementation with vitamin A or beta-carotene during the child-bearing years reduced all-cause maternal mortality and, in night blind women, also infant mortality. The present trial is testing the efficacy of the same supplements from ~9 weeks' gestation to 12 weeks postpartum. The planned sample size is 68,000 pregnancies. It is being conducted in 19 rural unions, covering an area of ~750 sq km with a population of ~580,000 in Gaibandha and Southern Rangpur Districts in Northern Bangladesh. The study area was mapped as 596 "sectors" (unit of randomization), each comprising 200-275 households; ~135,000 houses were numerically addressed and, at the outset, 103,000 women were listed. Women are visited at home every 5 weeks by 596 trained female staff to detect pregnancy by a combination of menstrual history and urine testing. Newly married women are prospectively enlisted for pregnancy surveillance. Following informed consent urine-positive (pregnant) women detected during surveillance are enrolled to receive weekly a capsule containing 7000 retinol equivalents of preformed vitamin A, 42 mg of beta-carotene or placebo. Vital events are recorded weekly through 3 months postpartum. Trained interviewers conduct maternal nutritional and health and household socioeconomic assessments in the 1st trimester. At 3 months postpartum, interviewers assess both mother and infant for health and nutritional status, including apparent birth defects that are later physician-confirmed. An additional home health assessment occurs at 6 months post partum, and vital status is recorded for mother and infant at one year postpartum. A ~3% subsample of enrolled pregnant women participate in a substudy involving enhanced clinical, anthropometric, biochemical, body compositional, morbidity and interview-based assessment protocols in the 1st, 2nd and 3rd trimesters, and at 3 months post-partum. Reported maternal and infant deaths are verified and causes ascertained during "verbal autopsy" interviews with family members of the deceased.
Eligibility| Ages Eligible for Study: | 15 Years to 49 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Contact: Keith P West, Jr., Dr.P.H. | 410-955-2061 | kwest@jhsph.edu |
| Contact: Parul Christian, Dr.P.H. | 410-955-1188 | pchristi@jhsph.edu |
| Bangladesh, Rajshahi Division | |
| JiVitA Bangladesh Project | Recruiting |
| Rangpur, Rajshahi Division, Bangladesh | |
| Contact: Alain B Labrique, MSc 880-521-63391 alabriqu@jhsph.edu | |
| Contact: Keith P West, Jr., Dr.P.H. 410-955-2061 kwest@jhsph.edu | |
| Sub-Investigator: Joanne Katz, Sc.D. | |
| Sub-Investigator: Ahmed Shamim, M.Sc. | |
| Sub-Investigator: Emorn Wasantwisut, Ph.D. | |
| Principal Investigator: | Keith P West, Jr., Dr.P.H. | Johns Hopkins Bloomberg School of Public Health |
| Study Director: | Parul Christian, Dr.P.H. | Johns Hopkins Bloomberg School of Public Health |
| Study Director: | Rolf DW Klemm, Dr.P.H. | Johns Hopkins Bloomberg School of Public Health |
| Study Director: | Mahbubur Rashid, MBBS, MSc | JiVitA Bangladesh Project |
| Study Director: | Alain B Labrique, MSc | Johns Hopkins Bloomberg School of Public Health |
| Study Director: | Alfred Sommer, M.D. | Johns Hopkins Bloomberg School of Public Health |
More Information
| Study ID Numbers: | GHS-A-00-03-00019-00 |
| Study First Received: | September 12, 2005 |
| Last Updated: | September 6, 2006 |
| ClinicalTrials.gov Identifier: | NCT00198822 History of Changes |
| Health Authority: | United States: Institutional Review Board; Bangladesh: National Integrated Program in Health and Population, Ministry of Health and Family Welfare |
|
Maternal mortality Infant mortality Vitamin A Beta-carotene |
Micronutrients Bangladesh Perinatal mortality Neonatal mortality |
|
Anticarcinogenic Agents Vitamin A Deficiency Night Blindness Beta Carotene Antioxidants Vision Disorders Molecular Mechanisms of Pharmacological Action Antineoplastic Agents Avitaminosis Growth Substances Eye Diseases Physiological Effects of Drugs |
Protective Agents Pharmacologic Actions Malnutrition Retinol palmitate Therapeutic Uses Vitamin A Vitamins Nutrition Disorders Micronutrients Carotenoids Deficiency Diseases |