Diarrhea Clinical Trial
— ShigOraVaxOfficial title:
A Baseline Study in Support of Clinical Evaluation of an Oral Shigella Vaccine Development in Africa
Verified date | July 2022 |
Source | Centre for Infectious Disease Research in Zambia |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
This study aims to address the paucity of accurate incidence data of diarrheal diseases associated with Shigella in Zambia and Burkina Faso. Given the limited feasibility of the current complex diagnostic methods used to detect Shigella in endemic and developing countries due to the costs, the none availability of reagents and a requirement of expensive and complex machinery, we suggest to use a rapide, easy-to-use, cost-effective, and robust Polymerase Chain Reaction (PCR) based rapid tool, the Loop-mediated isothermal amplification (LAMP) based diagnostic assay (ES-RLDT). This baseline study will enable us to generate an accurate estimate of Shigella incidence so as to inform future trials' designs of an oral vaccine development (ShigOraVax) in Burkina Faso and Zambia. This project is part of the EDCTP2 programme supported by the European Union under grant agreement "No RIA2018V-2308
Status | Completed |
Enrollment | 1334 |
Est. completion date | November 30, 2021 |
Est. primary completion date | November 30, 2021 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | N/A to 5 Years |
Eligibility | Inclusion Criteria: - Children who are under five years, are resident in the catchment areas of participating health facilities and whose parents or guardians have no anticipated plan to leave the area for the next 12 months; - Willing to submit child biological samples for testing and/or storage; - Parent or guardian providing written informed consenting to the study. Exclusion Criteria: - Any child born after the Census has taken place(Zambia) or whose household was not randomly selected from the database (Burkina Faso) - Current participation in a research with the use of any drug or vaccine. - Parent or guardian unwilling to provide consent - Any confirmed or suspected immunosuppressive or immuniodeficiency condition based on medical history and physical examination (No testing will be done for HIV) - A family history of congenital or hereditary immunodeficiency - Major congenital defects - Immunosuppresive therapy within 3 months prior to recruitment |
Country | Name | City | State |
---|---|---|---|
Burkina Faso | Schiphra Hospital | Ouagadougou | |
Zambia | Chainda South Health Facility | Lusaka | |
Zambia | Arthur Davidson Childrens Hospital | Ndola | Copperbelt |
Lead Sponsor | Collaborator |
---|---|
Centre for Infectious Disease Research in Zambia | European and Developing Countries Clinical Trials Partnership (EDCTP), European Vaccine Initiative, Groupe de Recherche Action en Sante |
Burkina Faso, Zambia,
GBD Diarrhoeal Diseases Collaborators. Estimates of global, regional, and national morbidity, mortality, and aetiologies of diarrhoeal diseases: a systematic analysis for the Global Burden of Disease Study 2015. Lancet Infect Dis. 2017 Sep;17(9):909-948. doi: 10.1016/S1473-3099(17)30276-1. Epub 2017 Jun 1. Erratum in: Lancet Infect Dis. 2017 Sep;17(9):897. — View Citation
Kotloff KL, Winickoff JP, Ivanoff B, Clemens JD, Swerdlow DL, Sansonetti PJ, Adak GK, Levine MM. Global burden of Shigella infections: implications for vaccine development and implementation of control strategies. Bull World Health Organ. 1999;77(8):651-66. — View Citation
Platts-Mills JA, Liu J, Rogawski ET, Kabir F, Lertsethtakarn P, Siguas M, Khan SS, Praharaj I, Murei A, Nshama R, Mujaga B, Havt A, Maciel IA, McMurry TL, Operario DJ, Taniuchi M, Gratz J, Stroup SE, Roberts JH, Kalam A, Aziz F, Qureshi S, Islam MO, Sakpaisal P, Silapong S, Yori PP, Rajendiran R, Benny B, McGrath M, McCormick BJJ, Seidman JC, Lang D, Gottlieb M, Guerrant RL, Lima AAM, Leite JP, Samie A, Bessong PO, Page N, Bodhidatta L, Mason C, Shrestha S, Kiwelu I, Mduma ER, Iqbal NT, Bhutta ZA, Ahmed T, Haque R, Kang G, Kosek MN, Houpt ER; MAL-ED Network Investigators. Use of quantitative molecular diagnostic methods to assess the aetiology, burden, and clinical characteristics of diarrhoea in children in low-resource settings: a reanalysis of the MAL-ED cohort study. Lancet Glob Health. 2018 Dec;6(12):e1309-e1318. doi: 10.1016/S2214-109X(18)30349-8. Epub 2018 Oct 1. — View Citation
Song T, Toma C, Nakasone N, Iwanaga M. Sensitive and rapid detection of Shigella and enteroinvasive Escherichia coli by a loop-mediated isothermal amplification method. FEMS Microbiol Lett. 2005 Feb 1;243(1):259-63. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Incidence of Shigella diarrheal disease in children under fives in Zambia and Burkina Faso | number of children testing Shigella positive during course of study | 1 year | |
Secondary | Attributable fraction for Shigella among all-cause MSD in children under 5 years | the number of children presenting with MSD with confirmed Shigella | 1 year | |
Secondary | Incidence of ETEC diarrheal disease in children under fives in Zambia and Burkina Faso | the number of children presenting with MSD with confirmed ETEC | 1 year | |
Secondary | Antimicrobial susceptibility/resistance of isolates to common antibiotics | Proportion of shigella isolates resistant to common antibiotics | 1 year | |
Secondary | Predictive accuracy of the modified diarrhoea severity scoring tool among children presenting with MSD | Proportion of MSD cases confirmed by the modified severity score | 1 year |
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