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

BACKGROUND: 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 oc...

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Autores principales: Guwatudde, David, Ezeamama, Amara E, Bagenda, Danstan, Kyeyune, Rachel, Wabwire-Mangen, Fred, Wamani, Henry, Mugusi, Ferdinand, Spiegelman, Donna, Wang, Molin, Manabe, Yukari C, Fawzi, Wafaie W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3519743/
https://www.ncbi.nlm.nih.gov/pubmed/23151221
http://dx.doi.org/10.1186/1471-2334-12-304
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author Guwatudde, David
Ezeamama, Amara E
Bagenda, Danstan
Kyeyune, Rachel
Wabwire-Mangen, Fred
Wamani, Henry
Mugusi, Ferdinand
Spiegelman, Donna
Wang, Molin
Manabe, Yukari C
Fawzi, Wafaie W
author_facet Guwatudde, David
Ezeamama, Amara E
Bagenda, Danstan
Kyeyune, Rachel
Wabwire-Mangen, Fred
Wamani, Henry
Mugusi, Ferdinand
Spiegelman, Donna
Wang, Molin
Manabe, Yukari C
Fawzi, Wafaie W
author_sort Guwatudde, David
collection PubMed
description BACKGROUND: 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. TRIAL REGISTRATION: Clinical Trial Registration-URL: http://www.clinicaltrials.gov. Unique identifier: NCT01228578
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spelling pubmed-35197432012-12-12 Multivitamin supplementation in HIV infected adults initiating antiretroviral therapy in Uganda: the protocol for a randomized double blinded placebo controlled efficacy trial Guwatudde, David Ezeamama, Amara E Bagenda, Danstan Kyeyune, Rachel Wabwire-Mangen, Fred Wamani, Henry Mugusi, Ferdinand Spiegelman, Donna Wang, Molin Manabe, Yukari C Fawzi, Wafaie W BMC Infect Dis Study Protocol BACKGROUND: 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. TRIAL REGISTRATION: Clinical Trial Registration-URL: http://www.clinicaltrials.gov. Unique identifier: NCT01228578 BioMed Central 2012-11-15 /pmc/articles/PMC3519743/ /pubmed/23151221 http://dx.doi.org/10.1186/1471-2334-12-304 Text en Copyright ©2012 Guwatudde et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Study Protocol
Guwatudde, David
Ezeamama, Amara E
Bagenda, Danstan
Kyeyune, Rachel
Wabwire-Mangen, Fred
Wamani, Henry
Mugusi, Ferdinand
Spiegelman, Donna
Wang, Molin
Manabe, Yukari C
Fawzi, Wafaie W
Multivitamin supplementation in HIV infected adults initiating antiretroviral therapy in Uganda: the protocol for a randomized double blinded placebo controlled efficacy trial
title Multivitamin supplementation in HIV infected adults initiating antiretroviral therapy in Uganda: the protocol for a randomized double blinded placebo controlled efficacy trial
title_full Multivitamin supplementation in HIV infected adults initiating antiretroviral therapy in Uganda: the protocol for a randomized double blinded placebo controlled efficacy trial
title_fullStr Multivitamin supplementation in HIV infected adults initiating antiretroviral therapy in Uganda: the protocol for a randomized double blinded placebo controlled efficacy trial
title_full_unstemmed Multivitamin supplementation in HIV infected adults initiating antiretroviral therapy in Uganda: the protocol for a randomized double blinded placebo controlled efficacy trial
title_short Multivitamin supplementation in HIV infected adults initiating antiretroviral therapy in Uganda: the protocol for a randomized double blinded placebo controlled efficacy trial
title_sort multivitamin supplementation in hiv infected adults initiating antiretroviral therapy in uganda: the protocol for a randomized double blinded placebo controlled efficacy trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3519743/
https://www.ncbi.nlm.nih.gov/pubmed/23151221
http://dx.doi.org/10.1186/1471-2334-12-304
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