Overview
Controlled Trial of Prenatal Vitamin D3 Supplementation to Prevent Vitamin D Deficiency in Mothers and Their Infants
Status:
Completed
Completed
Trial end date:
2012-04-01
2012-04-01
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
The purpose of this research study is to compare the effects of higher dose vitamin D with commonly recommended dose in pregnant women to see which is better in achieving and/or maintaining sufficient vitamin D blood levels during pregnancy and in newborn infants as well as improving growth in the infant.Phase:
Phase 3Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Children's Hospital Medical Center, CincinnatiCollaborators:
Thrasher Research Fund
United Arab Emirates UniversityTreatments:
Cholecalciferol
Ergocalciferols
Vitamin D
Vitamins
Criteria
Inclusion Criteria:- Women who are within the ages of 18-45 years
- In good general health
- 12 weeks pregnant (based on last menstrual period)
Exclusion Criteria:
- Mothers with preexisting type I or type II diabetes
- Mothers with preexisting hypertension
- Mothers with preexisting parathyroid disease or uncontrolled thyroid disease
- Mothers with multiple fetuses (e.g., twins, triplets, etc.)