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CompletedNCT00356824Updated Nov 1, 2021

Relationship Between HIV and Malaria in Ugandan Children

An observational study in HIV Infections and Malaria, sponsored by National Institute of Allergy and Infectious Diseases (NIAID). Completed at 1 site in Uganda. Open to participants aged 1 Year to 10 Years. Per ClinicalTrials.gov, last updated 2021-11-01.

Sponsored by National Institute of Allergy and Infectious Diseases (NIAID) · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
300
Ages
1 Year to 10 Years
Sex
All
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Study summary

HIV and malaria are two of the most important diseases to afflict children in sub-Saharan Africa. However, it is unknown what relationships exist between the two diseases. The purpose of this study is to determine the relationship between HIV and malaria infections in HIV infected Ugandan children.

Read the detailed description

HIV and malaria are two of the most important infectious diseases in sub-Saharan Africa. By 2000, over 25 million children and adults were living with HIV/AIDS, and 16 million people had died of the disease. Malaria is also of great importance in Africa, where over 90% of the 500 million annual cases and 2.7 million annual deaths occur primarily in children under the age of 5. Any interaction between these two diseases is of tremendous public health importance; however, data in this area, especially information on the relevance of HIV and malaria coinfection, are limited. Little is known about HIV infection's effects on antimalarial therapy, the effects of anti-HIV treatment on malaria incidence and treatment outcomes, and the effect of malaria on HIV disease progression. This study will examine HIV infected children in Uganda and evaluate these relationships between HIV and malaria.

This study will last 4 years. All participants will receive TMP/SMX as prophylaxis for malaria throughout this study. Children will be treated for all episodes of uncomplicated malaria with amodiaquine and artesunate; this treatment for malaria will be provided. Antiretroviral treatment for HIV, if deemed necessary by the study physician, will not be provided through this study. In the case of missed scheduled visits at the clinic, children and their parents or guardians will be visited at home by study staff, who will then bring the children and their parents and guardians to the clinic for their appointments.

Parents or guardians will be asked to bring children to the study clinic for all medical care. Unless instructed otherwise, the study clinic should be the only place where children in this study receive care and medications for the duration of the study. At each study visit for a new illness, children who have a temperature of 38 C (100.4 F) or greater, report having a fever in the 24 hours prior to the visit, or have suspected malaria will have their blood collected to check for malaria. If the blood is negative for malaria, the child will be treated with standard of care for the non-malaria illness in the Mulago Hospital complex.

If the blood is positive for malaria, the child will be classified as having either uncomplicated or complicated malaria. In cases of uncomplicated malaria, children will undergo medical history, a physical exam, and additional blood collection on the day of diagnosis (Day 0). Doses of amodiaquine and artesunate will be given once a day for 3 days in the study clinic by a study nurse, who will directly observe the child taking the medication. Study visits associated with uncomplicated malaria will occur on Days 1, 2, 3, 7, 14, 28, and any other day when the child feels ill; a physical exam and blood collection to check for malaria will occur at all visits. In cases of complicated malaria, children will be treated with quinine and will be referred to the Acute Care Unit of the Mulago Hospital complex.

Regardless of health during the course of the study, children will need to return to the clinic every 30 days to undergo a physical exam and blood collection to check for malaria. If malaria is found, children will undergo the 14-day standardized follow-up period as described above. At least every 3 months, additional blood collection will occur to determine HIV viral load, liver and kidney function, and immune parameters.

As of 07/01/08, all study participants with malaria will receive standard of care treatment through the Pediatric Infectious Disease Clinic. No treatment will be provided by the study.

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Conditions studied

  • HIV Infections
  • Malaria

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Keywords

  • Child
03

In context

Malaria

1,299 studies on the registry are indexed under Malaria; 86 are open to participants now.

This study's planned enrollment of 300 is below the median of 600 across 218 observational studies indexed under Malaria.

Browse Malaria studies →

Lead sponsor

National Institute of Allergy and Infectious Diseases (NIAID) is the lead sponsor of 2,401 studies on the registry; 179 are open to participants now.

Of its 396 completed or terminated interventional studies of FDA-regulated products, 294 (74%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
1 Year to 10 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

HIV-infected children in Ugana at risk for malaria infection

Inclusion criteria

  • HIV infected
  • Resides within a 20 km (12.4 mi) radius of the study clinic in Kampala, Uganda
  • Had a minimum of 1 regularly scheduled clinic visit in the 3 months prior to study entry
  • Willing to return to the study clinic if fever or other illness occurs during this study
  • Willing to avoid medications administered outside the Mulago Hospital Complex
  • Parent or guardian willing to provide informed consent

Exclusion criteria

Exclusion Criteria:

  • Intends to move more than 20 km (12.4 mi) from the study clinic during the follow-up period
  • Weigh less than 5 kg (11 lbs)
  • Participating in another Infectious Disease Clinic (IDC) cohort study
  • Any current medical problem requiring in-patient evaluation or home care
  • History of allergy or sensitivity to amodiaquine, artesunate, or quinine
  • Life-threatening screening laboratory values in the absence of malaria. More information on this criterion can be found in the protocol.
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
300 participants (estimated)
Biospecimen retention
Samples with dna

Groups and cohorts

  • 1

    HIV-infected children in Uganda

    Drug: Amodiaquine · Drug: Artesunate

Interventions

  • DrugAmodiaquine

    200 mg oral tablet taken daily for 3 days under direct supervision at study clinic

    Also known as: Camoquin

  • DrugArtesunate

    50 mg oral tablet taken daily for 3 days under direct supervision at study clinic

    Also known as: Arsumax

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Study locations

1 site
  • Pediatric Infectious Diseases Clinic, Mulago Hospital Complex
    Kampala, Uganda
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References and documents

Publications

  • Corbett EL, Steketee RW, ter Kuile FO, Latif AS, Kamali A, Hayes RJ. HIV-1/AIDS and the control of other infectious diseases in Africa. Lancet. 2002 Jun 22;359(9324):2177-87. doi: 10.1016/S0140-6736(02)09095-5. Erratum In: Lancet 2002 Oct 12;360(9340):1178. PubMed 12090997 ↗
  • Harms G, Feldmeier H. HIV infection and tropical parasitic diseases - deleterious interactions in both directions? Trop Med Int Health. 2002 Jun;7(6):479-88. doi: 10.1046/j.1365-3156.2002.00893.x. PubMed 12031069 ↗
  • Kalyesubula I, Musoke-Mudido P, Marum L, Bagenda D, Aceng E, Ndugwa C, Olness K. Effects of malaria infection in human immunodeficiency virus type 1-infected Ugandan children. Pediatr Infect Dis J. 1997 Sep;16(9):876-81. doi: 10.1097/00006454-199709000-00011. PubMed 9306483 ↗
  • Rowland-Jones SL, Lohman B. Interactions between malaria and HIV infection-an emerging public health problem? Microbes Infect. 2002 Oct;4(12):1265-70. doi: 10.1016/s1286-4579(02)01655-6. PubMed 12467769 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 1, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00356824
Lead sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
First posted
Jul 26, 2006
Start date
Nov 2005
Primary completion
Apr 2007
Completion
May 2010
Last update
Nov 1, 2021

Study contacts

Diane V. Havlir, MD
principal investigator · University of California, San Francisco and San Francisco General Hospital
Moses R. Kamya, MBChB, MMed, MPH
principal investigator · Department of Medicine, Makerere University, Kampala, Uganda
Rukyalekere-Adeodadata Kekitiinwa
principal investigator · Department of Pediatrics, Makerere University, Kampala, Uganda
Anne Gasasira
principal investigator · Makerere University Medical School, Makerere University, Kampala, Uganda
Israel Kalyesubula
principal investigator · Department of Pediatrics, Makerere University, Kampala, Uganda
Grant Dorsey
principal investigator · University of California, San Francisco
Edwin Charlebois
principal investigator · University of California, San Francisco
Philip Rosenthal
principal investigator · University of California, San Francisco
Huyen Cao
principal investigator · California Department of Human Services
View the source record on ClinicalTrials.gov ↗

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