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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01229189
Other study ID # Vitamin D Study
Secondary ID
Status Completed
Phase N/A
First received October 26, 2010
Last updated March 7, 2012
Start date February 2010
Est. completion date August 2011

Study information

Verified date March 2012
Source Aga Khan University
Contact n/a
Is FDA regulated No
Health authority Pakistan: Ministry of Health
Study type Interventional

Clinical Trial Summary

Vitamin D deficiency is wide spread in South Asian population and is contributing to burden of disease in this region including Pakistan. The relative importance of vitamin D deficiency, mutation in its receptor and maternal and child health has not been established in Pakistan and population based studies are required to explore and avert the maternal and Neonatal complications and consequences of Vitamin D deficiency

The trial will evaluate the effectiveness of Vitamin D supplementation to pregnant women and their Infants. It will be a double blind placebo controlled trial, which will be conducted in a rural district of Pakistan.


Description:

The investigators are proposing a community based introduction of vitamin D supplementation and we intend to understand the complex relationship between vitamin D, the growth factors and maternal and infant anthropometric variables and hope to unravel the reasons of vitamin D deficiency in our population.

The investigators expect that if vitamin D is supplemented to pregnant women and their newborn infants it will inevitably replenish the micronutrient stores and aid to resolve the maternal and neonatal morbidity due to Vitamin D deficiency.


Recruitment information / eligibility

Status Completed
Enrollment 460
Est. completion date August 2011
Est. primary completion date August 2011
Accepts healthy volunteers No
Gender Female
Age group 15 Years to 49 Years
Eligibility Inclusion Criteria:

- Pregnant women from 20-22 weeks of gestation and their infants, who will agree to take part in this study, will be enrolled.

Exclusion Criteria:

- Pregnant women with pre existing type 1 or type II diabetes

- Women with multiple fetuses, babies (twins, triplets)

- Pregnant women with high level of Vitamin D

- Babies with multiple congenital anomalies

- Babies with serious birth injury, birth asphyxia and serious infections

- Low birth weight less than 1.5

- Refuse to participate in the study

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Health Services Research


Intervention

Dietary Supplement:
Vitamin D
Maternal dose of 4000 IU daily for 20 weeks Neonatal dose of 400 IU daily for 24 weeks
Placebo
Placebo will be supplemented to pregnant women and their neonates in the same pattern as in intervention group.

Locations

Country Name City State
Pakistan Project Office Aga Khan University Pind Dadan Khan Punjab

Sponsors (2)

Lead Sponsor Collaborator
Aga Khan University John Snow, Inc.

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Maternal and Neonatal complications Preeclampsia, hypertension ,poor weight gain etc during pregnancy.Still birth rates, Rate of low birth weight, prematurity,Neonatal seizures, Infants with growth failure, signs and symptoms of vitamin D deficiency. Infants with infections: pneumonia, diarrhea and Receptor polymorphism six months post enrolement No
Secondary Prevalence and Risk factors for Maternal and Neonatal Vit D Deficiency Six months post recruitment No
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