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The Mirasol Evaluation of Reduction in Infections Trial (MERIT): study protocol for a randomized controlled clinical trial.
Kasirye, Ronnie; Hume, Heather A; Bloch, Evan M; Lubega, Irene; Kyeyune, Dorothy; Shrestha, Ruchee; Ddungu, Henry; Musana, Hellen Wambongo; Dhabangi, Aggrey; Ouma, Joseph; Eroju, Priscilla; de Lange, Telsa; Tartakovsky, Michael; White, Jodie L; Kakura, Ceasar; Fowler, Mary Glenn; Musoke, Philippa; Nolan, Monica; Grabowski, M Kate; Moulton, Lawrence H; Stramer, Susan L; Whitby, Denise; Zimmerman, Peter A; Wabwire, Deo; Kajja, Isaac; McCullough, Jeffrey; Goodrich, Raymond; Quinn, Thomas C; Cortes, Robert; Ness, Paul M; Tobian, Aaron A R.
Afiliación
  • Kasirye R; MUJHU Research Collaboration, Kampala, Uganda.
  • Hume HA; Department of Pediatrics, University of Montreal, Montréal, QC, Canada.
  • Bloch EM; Department of Pathology, School of Medicine, Johns Hopkins University, Baltimore, MD, USA.
  • Lubega I; MUJHU Research Collaboration, Kampala, Uganda.
  • Kyeyune D; Uganda Blood Transfusion Services, Kampala, Uganda.
  • Shrestha R; Department of Pathology, School of Medicine, Johns Hopkins University, Baltimore, MD, USA.
  • Ddungu H; Uganda Cancer Institute, Kampala, Uganda.
  • Musana HW; MUJHU Research Collaboration, Kampala, Uganda.
  • Dhabangi A; Child Health and Development Centre, Makerere University College of Health Sciences, Kampala, Uganda.
  • Ouma J; MUJHU Research Collaboration, Kampala, Uganda.
  • Eroju P; MUJHU Research Collaboration, Kampala, Uganda.
  • de Lange T; National Institute of Allergy and Infectious Diseases Office of Cyber Infrastructure and Computational Biology, Bethesda, MD, USA.
  • Tartakovsky M; National Institute of Allergy and Infectious Diseases Office of Cyber Infrastructure and Computational Biology, Bethesda, MD, USA.
  • White JL; Department of Pathology, School of Medicine, Johns Hopkins University, Baltimore, MD, USA.
  • Kakura C; MUJHU Research Collaboration, Kampala, Uganda.
  • Fowler MG; Department of Pathology, School of Medicine, Johns Hopkins University, Baltimore, MD, USA.
  • Musoke P; Makerere University, Kampala, Uganda.
  • Nolan M; MUJHU Research Collaboration, Kampala, Uganda.
  • Grabowski MK; Department of Pathology, School of Medicine, Johns Hopkins University, Baltimore, MD, USA.
  • Moulton LH; Department of International Health, School of Public Health, Johns Hopkins University, Baltimore, MD, USA.
  • Stramer SL; Department of Scientific Affairs, American Red Cross, Gaithersburg, MD, USA.
  • Whitby D; Leidos Biomedical Research, AIDS and Cancer Virus Program, Frederick National Laboratory for Cancer Research, Frederick, MD, USA.
  • Zimmerman PA; The Center for Global Health & Diseases, Pathology Department, Case Western Reserve University, Cleveland, OH, USA.
  • Wabwire D; MUJHU Research Collaboration, Kampala, Uganda.
  • Kajja I; Department of Orthopaedics, Makerere University College of Health Sciences, Kampala, Uganda.
  • McCullough J; College of Health Solutions, Arizona State University, Phoenix, AZ, USA.
  • Goodrich R; Department of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, CO, USA.
  • Quinn TC; Department of Pathology, School of Medicine, Johns Hopkins University, Baltimore, MD, USA.
  • Cortes R; Department of International Health, School of Public Health, Johns Hopkins University, Baltimore, MD, USA.
  • Ness PM; Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
  • Tobian AAR; Terumo BCT, Lakewood, CO, USA.
Trials ; 23(1): 257, 2022 Apr 04.
Article en En | MEDLINE | ID: mdl-35379302
ABSTRACT

BACKGROUND:

Transfusion-transmitted infections (TTIs) are a global health challenge. One new approach to reduce TTIs is the use of pathogen reduction technology (PRT). In vitro, Mirasol PRT reduces the infectious load in whole blood (WB) by at least 99%. However, there are limited in vivo data on the safety and efficacy of Mirasol PRT. The objective of the Mirasol Evaluation of Reduction in Infections Trial (MERIT) is to investigate whether Mirasol PRT of WB can prevent seven targeted TTIs (malaria, bacteria, human immunodeficiency virus, hepatitis B virus, hepatitis C virus, hepatitis E virus, and human herpesvirus 8).

METHODS:

MERIT is a randomized, double-blinded, controlled clinical trial. Recruitment started in November 2019 and is expected to end in 2024. Consenting participants who require transfusion as medically indicated at three hospitals in Kampala, Uganda, will be randomized to receive either Mirasol-treated WB (n = 1000) or standard WB (n = 1000). TTI testing will be performed on donor units and recipients (pre-transfusion and day 2, day 7, week 4, and week 10 after transfusion). The primary endpoint is the cumulative incidence of one or more targeted TTIs from the Mirasol-treated WB vs. standard WB in a previously negative recipient for the specific TTI that is also detected in the donor unit. Log-binomial regression models will be used to estimate the relative risk reduction of a TTI by 10 weeks associated with Mirasol PRT. The clinical effectiveness of Mirasol WB compared to standard WB products in recipients will also be evaluated.

DISCUSSION:

Screening infrastructure for TTIs in low-resource settings has gaps, even for major TTIs. PRT presents a fast, potentially cost-effective, and easy-to-use technology to improve blood safety. MERIT is the largest clinical trial designed to evaluate the use of Mirasol PRT for WB. In addition, this trial will provide data on TTIs in Uganda. TRIAL REGISTRATION Mirasol Evaluation of Reduction in Infections Trial (MERIT) NCT03737669 . Registered on 9 November 2018.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Reacción a la Transfusión Tipo de estudio: Clinical_trials / Etiology_studies / Guideline Límite: Humans País/Región como asunto: Africa Idioma: En Revista: Trials Asunto de la revista: MEDICINA / TERAPEUTICA Año: 2022 Tipo del documento: Article País de afiliación: Uganda

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Reacción a la Transfusión Tipo de estudio: Clinical_trials / Etiology_studies / Guideline Límite: Humans País/Región como asunto: Africa Idioma: En Revista: Trials Asunto de la revista: MEDICINA / TERAPEUTICA Año: 2022 Tipo del documento: Article País de afiliación: Uganda