[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100614268":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":20,"centralContacts":25,"locations":33,"responsibleParty":68,"collaborators":10,"id":70,"slug":71,"hasResults":72,"nctId":73,"briefTitle":74,"officialTitle":75,"acronym":10,"eligibilityCriteria":76,"healthyVolunteers":72,"sex":77,"minAge":78,"maxAge":10,"enrollmentInfo":79,"targetDuration":82,"studyType":83,"phases":10,"briefSummary":84,"conditions":85,"keywords":87,"overallStatus":48,"whyStopped":10,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":103,"locationsCount":104},{"fullName":5,"class":6},"Instituto de Investigación Biomédica de Salamanca","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"High-risk FN cohort",null,"Adult onco-hematologic inpatients meeting inclusion criteria; two plasma draws at fever onset and 48 h.",[13],"Biological: Plasma and DNA sample collection for proteomic and genomic analysis",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":10},"BIOLOGICAL","Plasma and DNA sample collection for proteomic and genomic analysis","Collection of 10 mL of peripheral blood in EDTA tubes at fever onset (before antibiotic initiation) and 48 hours later for proteomic and genomic analysis. Samples are processed to obtain plasma and DNA, which will be used for mass spectrometry-based proteomics and potential metagenomic studies.",[9],[21],{"name":22,"affiliation":23,"role":24},"Jesús Francisco Bermejo Martín, MD PhD","Centro Asistencial Universitario de Salamanca (CAUSA)","PRINCIPAL_INVESTIGATOR",[26,30],{"name":22,"role":27,"phone":28,"phoneExt":10,"email":29},"CONTACT","+34923 29 45 41","jfbermejo@usal.es",{"name":31,"role":27,"phone":28,"phoneExt":10,"email":32},"Nadia García Mateo, PhD","nadiagarciamateo@ibsal.es",[34,46,59],{"facility":35,"status":36,"city":37,"state":37,"zip":10,"country":38,"countryCode":39,"cosmosGeoPoint":40,"geoPoint":45,"contacts":10},"Hospital Universitari Vall d'Hebron","NOT_YET_RECRUITING","Barcelona","Spain","ES",{"type":41,"coordinates":42},"Point",[43,44],2.15899,41.38879,{"lat":44,"lon":43},{"facility":47,"status":48,"city":49,"state":49,"zip":50,"country":38,"countryCode":39,"cosmosGeoPoint":51,"geoPoint":55,"contacts":56},"Complejo Asistencial Universitario de Salamanca","RECRUITING","Salamanca","37007",{"type":41,"coordinates":52},[53,54],-5.66388,40.96882,{"lat":54,"lon":53},[57],{"name":58,"role":27,"phone":28,"phoneExt":10,"email":29},"Jesús Francisco Bermejo Martín, PhD",{"facility":60,"status":36,"city":61,"state":62,"zip":10,"country":38,"countryCode":39,"cosmosGeoPoint":63,"geoPoint":67,"contacts":10},"Hospital Universitario Virgen Macarena","Seville","Sevilla",{"type":41,"coordinates":64},[65,66],-5.97317,37.38283,{"lat":66,"lon":65},{"type":69,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100614268","plasma-host-microbe-proteomics-to-predict-complications-in-high-risk-febrile-neutropenia-100614268",false,"NCT07277387","Plasma Host-Microbe Proteomics to Predict Complications in High-risk Febrile Neutropenia","A Multicenter Prospective Observational Study on the Plasma Proteomic Profiling of Human and Microbial Proteins for the Early Identification of Biomarker Combinations (Combitypes) Associated With Complications in Oncohematologic Patients With Febrile Neutropenia","Inclusion Criteria:\n\n* Adults (≥18 years).\n* Written informed consent provided by patient or legal representative.\n* Diagnosis of hematologic malignancy under induction chemotherapy, post-allogeneic hematopoietic stem cell transplantation, or CAR-T therapy.\n* High-risk febrile neutropenia (ANC ≤ 100 cells\u002Fmm³, expected duration ≥ 7 days, or significant comorbidities).\n* Fever defined as oral temperature ≥38.3 °C once or ≥38.0 °C for ≥1 hour.\n* Hospitalized or requiring immediate admission at the time of FN diagnosis.\n\n  ´- Initial uncomplicated clinical presentation, with no previous infection or colonization by multidrug-resistant bacteria.\n* Eligible for initial monotherapy with broad-spectrum empirical antibiotic.\n* Availability for serial plasma sampling and clinical follow-up.\n\nExclusion Criteria:\n\n* Age \\\u003C18 years.\n* Low-risk FN according to MASCC\u002FCISNE criteria.\n* Initial sample collected after antibiotic administration.\n* Decline or inability to provide informed consent.\n* Any condition preventing safe participation or reliable sample collection.\n* Fever induced by noninfectious causes (considered as adjustment factor, not exclusion).","ALL","18 Years",{"count":80,"type":81},350,"ESTIMATED","30 Days","OBSERVATIONAL","Febrile neutropenia (FN) is a common oncologic emergency in patients with hematologic malignancies, associated with high morbidity and mortality. Early identification of patients at higher risk of complications such as sepsis or septic shock is critical to optimize antimicrobial management.\n\nThis study aims to characterize the human and microbial plasma proteome using high-resolution mass spectrometry to identify biomarker combinations (\"combitypes\") capable of predicting complications in oncohematologic patients with FN.\n\nA cohort of 350 adult patients with high-risk FN and initially uncomplicated clinical presentation will be enrolled across three tertiary hospitals. Plasma samples will be collected at fever onset (before antibiotic initiation) and after 48 hours. Proteomic data will be integrated with clinical information using multivariate and machine learning models to develop a predictive model for complications.",[86],"Febrile Neutropenia",[88,89,90,91,92,93,94],"febrile neutropenia","hematologic malignancy","proteomics","sepsis","biomarkers","septic shock","mass spectrometry","2026-06-11",{"date":97,"type":98},"2026-06-15","ACTUAL",{"date":100,"type":98},"2026-06-09",{"date":102,"type":81},"2029-01",{"name":5,"class":6},3]