Febrile Neutropenia Clinical Trials

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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

Status: Recruiting
Location: See all (3) locations...
Intervention Type: Biological
Study Type: Observational
SUMMARY

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. This 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. A 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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Adults (≥18 years).

• Written informed consent provided by patient or legal representative.

• Diagnosis of hematologic malignancy under induction chemotherapy, post-allogeneic hematopoietic stem cell transplantation, or CAR-T therapy.

• High-risk febrile neutropenia (ANC ≤ 100 cells/mm³, expected duration ≥ 7 days, or significant comorbidities).

• Fever defined as oral temperature ≥38.3 °C once or ≥38.0 °C for ≥1 hour.

• Hospitalized or requiring immediate admission at the time of FN diagnosis.

• ´- Initial uncomplicated clinical presentation, with no previous infection or colonization by multidrug-resistant bacteria.

• Eligible for initial monotherapy with broad-spectrum empirical antibiotic.

• Availability for serial plasma sampling and clinical follow-up.

Locations
Other Locations
Spain
Hospital Universitari Vall d'Hebron
NOT_YET_RECRUITING
Barcelona
Complejo Asistencial Universitario de Salamanca
RECRUITING
Salamanca
Hospital Universitario Virgen Macarena
NOT_YET_RECRUITING
Seville
Contact Information
Primary
Jesús Francisco Bermejo Martín, MD PhD
jfbermejo@usal.es
+34923 29 45 41
Backup
Nadia García Mateo, PhD
nadiagarciamateo@ibsal.es
+34923 29 45 41
Time Frame
Start Date: 2026-06-09
Estimated Completion Date: 2029-01
Participants
Target number of participants: 350
Treatments
High-risk FN cohort
Adult onco-hematologic inpatients meeting inclusion criteria; two plasma draws at fever onset and 48 h.
Sponsors
Leads: Instituto de Investigación Biomédica de Salamanca

This content was sourced from clinicaltrials.gov

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