Clinical Trials Directory

Trials / Unknown

UnknownNCT01684189

Registry of Febrile Neutropenia and Invasive Fungal Infections

A Non-interventional Prospective Registry to Monitor the Events of Febrile Neutropenia and Invasive Fungal Infections and the Diagnostic and Therapeutic Management in Patients With Malignant Hematologic Diseases After Chemotherapy

Status
Unknown
Phase
Study type
Observational
Enrollment
100 (estimated)
Sponsor
Chang Gung Memorial Hospital · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

Objectives: 1. To assess the percentage of febrile neutropenia and suspected fungal-related febrile episodes in patients receiving chemotherapy 2. To explore the percentage/distribution of infectious origins of febrile neutropenia 3. To explore the percentage/distribution of infectious pathogens of febrile neutropenia 4. To explore clinical outcomes of different infectious origins/pathogens in febrile neutropenia episodes 5. To have a clear view of therapeutic actions in the management of hematological patients with febrile neutropenia and suspected fungal-related febrile episodes

Detailed description

Objectives: 1. To assess the percentage of febrile neutropenia and suspected fungal-related febrile episodes in patients receiving chemotherapy 2. To explore the percentage/distribution of infectious origins of febrile neutropenia 3. To explore the percentage/distribution of infectious pathogens of febrile neutropenia 4. To explore clinical outcomes of different infectious origins/pathogens in febrile neutropenia episodes 5. To have a clear view of therapeutic actions in the management of hematological patients with febrile neutropenia and suspected fungal-related febrile episodes Study Design: * This is a single institute, prospective, non-interventional registry for monitoring events of febrile neutropenia in hematological patients * Patients with newly diagnosed malignant hematological diseases will be enrolled into this registry Study Procedures: Data collection will include patients' basic information, underlying disease, baseline blood chemistry and blood cell counts, antifungal prophylaxis, C/T regimens, neutrophils and other blood cells, fever diagnosis and infectious sites work-up, clinical response, microbiology (including bacteria and fungus culture), renal and liver function, clinical diagnosis, work-up and intensive procedures and results, antifungal and antibacterial agents (including dosage, duration, and route), other drugs used (including antivirals, antineoplastics, corticosteroids, immunomodulators), clinical significant changes Sample Size Calculation and Statistical Analysis: Approximately 100 febrile neutropenia episodes in 500 chemotherapy cycles will be collected. This is an observational and exploratory study without hypothesis tests. Study subjects will be collected and monitored under normal clinical practice, and the sample size will be limited due to the hospital scale and disease characteristic (the sample size calculation is inapplicable here). All evaluations will be shown by exploratory and descriptive data analysis. The number of cases for each investigative definition, the corresponding percentage and the 95% confidence interval will be described.

Conditions

Interventions

TypeNameDescription
OTHERPatient registryPatient registry without study intervention

Timeline

Start date
2011-11-01
Completion
2013-08-01
First posted
2012-09-12
Last updated
2012-09-12

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT01684189. Inclusion in this directory is not an endorsement.