Multivitamin supplementation in HIV infected adults initiating antiretroviral therapy in Uganda: the protocol for a randomized double blinded placebo controlled efficacy trial

dc.contributor.authorGuwatudde, D.
dc.contributor.authorEzeamama, A.E.
dc.contributor.authorBagenda, D.
dc.contributor.authorKyeyune, R.
dc.contributor.authorWabwire-Mangen, F.
dc.contributor.authorWamani, H.
dc.contributor.authorMugusi, F.
dc.contributor.authorSpiegelman, D.
dc.contributor.authorWang, M.
dc.contributor.authorManabe, Y.C.
dc.contributor.authorFawzi, W.W.
dc.date.accessioned2013-04-18T10:24:33Z
dc.date.available2013-04-18T10:24:33Z
dc.date.issued2012
dc.description.abstractBACKGROUND: Use of multivitamin supplements during the pre-HAART era has been found to reduce viral load, enhance immune response, and generally improve clinical outcomes among HIV-infected adults. However, immune reconstitution is incomplete and significant mortality and opportunistic infections occur in spite of HAART. There is insufficient research information on whether multivitamin supplementation may be beneficial as adjunct therapy for HIV-infected individuals taking HAART. We propose to evaluate the efficacy of a single recommended daily allowance (RDA) of micronutrients (including vitamins B-complex, C, and E) in slowing disease progression among HIV-infected adults receiving HAART in Uganda. METHODS/DESIGN: We are using a randomized, double-blind, placebo-controlled trial study design. Eligible patients are HIV-positive adults aged at least 18 years, and are randomized to receive either a placebo; or multivitamins that include a single RDA of the following vitamins: 1.4 mg B1, 1.4 mg B2, 1.9 mg B6, 2.6 mcg B12, 18 mg niacin, 70 mg C, 10 mg E, and 0.4 mg folic acid. Participants are followed for up to 18 months with evaluations at baseline, 6, 12 and 18 months. The study is primarily powered to examine the effects on immune reconstitution, weight gain, and quality of life. In addition, we will examine the effects on other secondary outcomes including the risks of development of new or recurrent disease progression event, including all-cause mortality; ARV regimen change from first- to second-line therapy; and other adverse events as indicated by incident peripheral neuropathy, severe anemia, or diarrhea. DISCUSSIONS: The conduct of this trial provides an opportunity to evaluate the potential benefits of this affordable adjunct therapy (multivitamin supplementation) among HIV-infected adults receiving HAART in a developing country setting.en_GB
dc.identifier.citationGuwatudde, D., Ezeamama, A. E., Bagenda, D., Kyeyune, R., Wabwire-Mangen, F., Wamani, H., ... & Fawzi, W. W. (2012). Multivitamin supplementation in HIV infected adults initiating antiretroviral therapy in Uganda: the protocol for a randomized double blinded placebo controlled efficacy trial. BMC infectious diseases, 12(1), 304.
dc.identifier.issn1471-2334/12/304
dc.identifier.otherdoi: 10.1186/1471-2334-12-304.
dc.identifier.urihttp://hdl.handle.net/123456789/864
dc.language.isoenen_GB
dc.publisherBMC Infectious Diseases
dc.relation.ispartofseriesBMC Infectious Diseases ;12:304
dc.subjectHIV infected adultsen_GB
dc.subjectHAARTen_GB
dc.subjectMicronutrient supplementationen_GB
dc.subjectNutritionen_GB
dc.subjectRandomized double-blind placebocontrolled trialen_GB
dc.subjectTrial protocol
dc.subjectUganda
dc.subjectSub-Saharan Africa
dc.titleMultivitamin supplementation in HIV infected adults initiating antiretroviral therapy in Uganda: the protocol for a randomized double blinded placebo controlled efficacy trialen_GB
dc.typeArticleen_GB

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