[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"ebola-hemorrhagic-fever\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:ebola-hemorrhagic-fever":22},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,35],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":4,"maxAge":4,"enrollmentInfo":16,"targetDuration":4,"studyType":19,"phases":4,"briefSummary":20,"conditions":21,"keywords":4,"overallStatus":23,"whyStopped":4,"lastUpdateSubmitDate":24,"lastUpdatePostDateStruct":25,"startDateStruct":28,"completionDateStruct":30,"leadSponsor":32,"locationsCount":4},"100646802","clinical-validation-of-isothermal-nucleic-acid-amplification-bioassays-modules---drc-100646802",false,"NCT07688083","Clinical Validation of Isothermal Nucleic Acid Amplification Bioassays Modules - DRC","Inclusion Criteria:\n\n* EBOV test positive and negative biobanked patient samples\n\nExclusion Criteria:\n\n* not applicable","ALL",{"count":17,"type":18},100,"ESTIMATED","OBSERVATIONAL","This study aims to validate the clinical performance of a newly developed isothermal nucleic acid amplification bioassay module for EBOV. A retrospective studies will be conducted using biobanked patient samples such as plasma samples and buccal swabs already collected by the Institut National de Recherches Biomédicales (INRB) in Kinshasa, DRC as part of their surveillance and outbreak activities. The diagnostic sensitivity and specificity of the EBOV bioassay module will be compared to the gold-standard reverse transcriptase polymerase chain reaction (RT-PCR) technologies used in the national reference lab.",[22],"Ebola Hemorrhagic Fever","NOT_YET_RECRUITING","2026-06-30",{"date":26,"type":27},"2026-07-07","ACTUAL",{"date":29,"type":18},"2027-01",{"date":31,"type":18},"2027-12",{"name":33,"class":34},"Institute of Tropical Medicine, Belgium","OTHER",{"id":36,"slug":37,"hasResults":11,"nctId":38,"briefTitle":39,"officialTitle":39,"acronym":4,"eligibilityCriteria":40,"healthyVolunteers":11,"sex":15,"minAge":4,"maxAge":4,"enrollmentInfo":41,"targetDuration":4,"studyType":19,"phases":4,"briefSummary":43,"conditions":44,"keywords":4,"overallStatus":23,"whyStopped":4,"lastUpdateSubmitDate":24,"lastUpdatePostDateStruct":46,"startDateStruct":48,"completionDateStruct":49,"leadSponsor":50,"locationsCount":4},"100645378","clinical-validation-of-isothermal-nucleic-acid-amplification-bioassays-modules---guinea-100645378","NCT07681752","Clinical Validation of Isothermal Nucleic Acid Amplification Bioassays Modules - GUINEA","Inclusion Criteria:\n\n* EBOV and LASV test positive and negative biobanked patient samples\n\nExclusion Criteria:\n\n* not applicable",{"count":42,"type":18},150,"This study aim to validate the clinical performances of two newly developed isothermal nucleic acid amplification bioassays modules for EBOV and LASV. Two retrospective studies will be conducted using biobanked patient samples such as plasma samples and buccal swabs already collected by the Centre de Recherche en Virologie, Laboratoire des Fièvres Hémorragiques Virales de Guinée (CRV-LFHVG) as part of their surveillance and outbreak activities. The diagnostic sensitivity and specificity of the EBOV and LASV bioassays modules will be compared to the gold-standard reverse transcriptase polymerase chain reaction (RT-PCR) technologies used in the national reference lab.",[22,45],"Lassa Hemorrhagic Fever",{"date":47,"type":27},"2026-07-02",{"date":29,"type":18},{"date":31,"type":18},{"name":33,"class":34}]