Evidence map›Paper›PMID 42817974›Full record

ArticleWellcome open research2025

Hydroxyurea - Pragmatic Reduction In Mortality and Economic burden (H-PRIME): A 2x2x2 factorial randomised open-label trial investigating practical approaches to the treatment of sickle cell disease at four sites in Eastern Uganda.

Peter Olupot-Olupot, Denis Amorut, Paul Ongodia, Charles B Okalebo, Julian Abeso, Florence Aloroker, Sarah Asio, Amos Odiit, Charles Kiyaga, Rita Muhindo and 13 more

Abstract read
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Article in Wellcome open research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

23 authors.

Peter Olupot-OlupotMbale Campus, Busitema University, Mbale, Eastern Region, Uganda.ORCID https://orcid.org/0000-0002-5757-609X
Denis AmorutMbale Clinical Research Institute, Mbale, Uganda.
Paul OngodiaMbale Clinical Research Institute, Mbale, Uganda.
Charles B OkaleboMbale Clinical Research Institute, Mbale, Uganda.
Julian AbesoMbale Clinical Research Institute, Mbale, Uganda.
Florence AlorokerMbale Clinical Research Institute, Mbale, Uganda.
Sarah AsioMbale Clinical Research Institute, Mbale, Uganda.
Amos OdiitMbale Clinical Research Institute, Mbale, Uganda.
Charles KiyagaUganda Central Public Health Laboratory, Kampala, Uganda.
Rita MuhindoMbale Clinical Research Institute, Mbale, Uganda.ORCID https://orcid.org/0000-0003-4252-5924
Sophie UyogaCentre for Geographic Medicine Research Coast, Kilifi, Kilifi County, Kenya.ORCID https://orcid.org/0000-0003-1746-7873
George MochamahCentre for Geographic Medicine Research Coast, Kilifi, Kilifi County, Kenya.
Asad MuyindaMbale Clinical Research Institute, Mbale, Uganda.
Grace AbongoMbale Clinical Research Institute, Mbale, Uganda.
Gideon NyutuCentre for Geographic Medicine Research Coast, Kilifi, Kilifi County, Kenya.
Christabel MogakaCentre for Geographic Medicine Research Coast, Kilifi, Kilifi County, Kenya.
Kathryn MaitlandMbale Campus, Busitema University, Mbale, Eastern Region, Uganda.
Diana GibbMedical Research Council Clinical Trials Unit at University College London, London, England, UK.ORCID https://orcid.org/0000-0002-9738-5490
Ann Sarah WalkerMedical Research Council Clinical Trials Unit at University College London, London, England, UK.
Roisin ConnonMedical Research Council Clinical Trials Unit at University College London, London, England, UK.ORCID https://orcid.org/0000-0002-4408-4336
Elizabeth GeorgeMedical Research Council Clinical Trials Unit at University College London, London, England, UK.
Russell E WareCincinnati Children's Hospital Pediatric Hematology and Global Health Center, Cincinnati, USA.
Thomas N WilliamsMbale Campus, Busitema University, Mbale, Eastern Region, Uganda.ORCID https://orcid.org/0000-0003-4456-2382

Funding

Wellcome Trust
6 · The paper itself

Abstract

Background: Sickle cell disease is the most common and severe genetic disease in humans worldwide. The majority of those affected are born in sub-Saharan Africa, where resources to diagnose and manage them are often limited. Fresh approaches to the pragmatic management of children with sickle cell disease in Africa that improve both morbidity and mortality are urgently needed. Methods: Hydroxyurea - Pragmatic Reduction In Mortality and Economic burden (H-PRIME) is a 2 × 2 × 2 factorial randomized open-label trial that is investigating three separate interventions. Eighteen hundred children aged 1-10 years attending sickle cell clinics at one of four sites in Eastern Uganda are being randomized to: (1) hydroxyurea administered at a low dose (10 mg/kg/day) versus high dose (25 mg/kg/day), prescribed pragmatically through a weight-band-based approach and with clinically, rather than laboratory-guided monitoring; (2) enhanced malaria prophylaxis with weekly doses of dihydroartemisinin-piperaquine versus monthly doses of sulfadoxine-pyrimethamine (standard of care); and (3) enhanced antibacterial prophylaxis with daily cotrimoxazole throughout life versus twice daily penicillin until the age of 5 years (standard of care). All children will be followed up for 48 months after the date on which the first child was randomized. The primary endpoint for the hydroxyurea randomization will be mortality, for the antimalarial random will be malaria-associated hospital admission, and for the antimicrobial randomization will be all-cause hospital admission. Secondary outcomes will include the incidence of sickle-specific complications, receipt of blood transfusions, hemoglobin and fetal hemoglobin concentrations, and economic costs and benefits of the three interventions. Conclusions: The first participant was recruited for the trial on January 16, 2024. In total, 1487 of the 1800 target children were recruited by February 17, 2025. H-PRIME will efficiently answer three important pragmatic questions regarding the management of children with sickle cell disease in Africa. Registration: PACTR number 202401802272880 (09/01/2024).ISRCTN15724013 (25/02/2020).

Indexed as

bacterial infectionshydroxyureamalariasickle cell diseaseUganda

Identifiers

PMID42817974
PMCPMC13620357

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.