None listed
Conditions
Interventions
Pregnant women in trial will be randomly allocated to recieve either 50000IU vitamin D oral tablet supplementation monthly or twice monthly from 20 weeks gestation until birth of baby.
Sponsors
Newtown Union Health Service
Study design
Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)
Eligibility
Sex/Gender
All
Age
0 to No maximum
Healthy volunteers
No
Inclusion criteria
Pregnant women seeking maternity care with midwifery services involved in the study.
Exclusion criteria
If antenatal Vitamin D level is > 75nmol/litre when enrolling in study
Outcome results
None listed