drugset / Trial / NCT02215213

Assessment of Dose Effectiveness of Vitamin D Supplementation During Pregnancy- a Dose Comparison Trial

NCT02215213

Completed 350 enrolled Aga Khan University
RandomizedParallel-groupDouble-blindPrevention

Summary

The study is randomized blinded trial of Vitamin D supplementation to pregnant women; the study participants will receive Vitamin D in supplement form. Pregnant women will be individually randomized to three groups receiving a dose of 400, 2000 and 4000 IU/ day till the time of delivery.A blood sample will also be collected from the participant at the time of recruitment /before the starting of the supplementation for the assessment of Calcium, Phosphorus, Alkaline Phosphatase and Vitamin D levels. The second blood sample for vitamin D level to assess vitamin D status will be done after completion of the supplementation phase at the time of delivery (till 48 hours of delivery). The samples will be sent to Aga Khan University laboratory

Timeline

Start
2013-06
Primary completion
2015-07
Completion
2016-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Vitamin D Other / unclassified 400 iu Oral
Comparator Vitamin D Other / unclassified 2000 iu Oral
Comparator Vitamin D Other / unclassified 4000 iu Oral

Indications