dc.contributor.author |
Manji, K.P. |
|
dc.contributor.author |
Sudfeld, C.R. |
|
dc.contributor.author |
Duggan, C.P. |
|
dc.contributor.author |
Aboud, S. |
|
dc.date.accessioned |
2019-03-07T08:01:33Z |
|
dc.date.available |
2019-03-07T08:01:33Z |
|
dc.date.issued |
2017 |
|
dc.identifier.citation |
Sudfeld, C.R., Manji, K.P., Duggan, C.P., Aboud, S., Muhihi, A., Sando, D.M., Al-Beity, F.M.A., Wang, M. and Fawzi, W.W., 2017. Effect of maternal vitamin D 3 supplementation on maternal health, birth outcomes, and infant growth among HIV-infected Tanzanian pregnant women: study protocol for a randomized controlled trial. Trials, 18(1), p.411. |
en_US |
dc.identifier.govdoc |
10.1186/s13063-017-2157-3 |
|
dc.identifier.uri |
http://dspace.muhas.ac.tz:8080/xmlui/handle/123456789/2293 |
|
dc.description.abstract |
Background: Vitamin D has significant immunomodulatory effects on both adaptive and innate immune responses. Observational studies indicate that adults infected with HIV with low vitamin D status may be at increased risk of mortality, pulmonary tuberculosis, and HIV disease progression. Growing observational evidence also suggests that low vitamin D status in pregnancy may increase the risk of adverse birth and infant health outcomes. As a result, antiretroviral therapy (ART) adjunct vitamin D3 supplementation may improve the health of
HIV-infected pregnant women and their children.
Methods/design: The Trial of Vitamins-5 (ToV5) is an individually randomized, double-blind, placebo-controlled trial of maternal vitamin D3 (cholecalciferol) supplementation conducted among 2300 HIV-infected pregnant women receiving triple-drug ART under Option B+ in Dar es Salaam, Tanzania. HIV-infected pregnant women of 12–27 weeks gestation are randomized to either: 1) 3000 IU vitamin D3 taken daily from randomization in pregnancy until trial discharge at 12 months postpartum; or 2) a matching placebo regimen. Maternal participants are followed-up at monthly clinic visits during pregnancy, at delivery, and then with their children at monthly postpartum clinic visits. The primary efficacy outcomes of the trial are: 1) maternal HIV disease progression or death; 2) risk of small-for-gestational age (SGA) births; and 3) risk of infant stunting at 1 year of age. The primary safety outcome of the trial is incident maternal hypercalcemia.
Secondary outcomes include a range of clinical and biological maternal and child health outcomes.
Discussion: The ToV5 will provide causal evidence on the effect of vitamin D3 supplementation on HIV progression and death, SGA births, and infant stunting at 1 year of age. The results of the trial are likely generalizable to HIV-infected pregnant women and their children in similar resource-limited settings utilizing the Option B+ approach.
Trial registration: ClinicalTrials.gov identifier: NCT02305927. Registered on 29 October 2014. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
BiomedCentral |
en_US |
dc.relation.ispartofseries |
Trials,;18(1), p.411. |
|
dc.subject |
Pulmonary tuberculosis |
en_US |
dc.subject |
HIV |
en_US |
dc.subject |
SGA births |
en_US |
dc.title |
Effect of Maternal Vitamin D3 Supplementation on Maternal Health, Birth Outcomes, and Infant Growth among HIV Infected Tanzanian Pregnant Women: Study Protocol for a Randomized Controlled Trial |
en_US |
dc.type |
Article |
en_US |