Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
OBSERVATIONAL
Brief Summary
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In each event of febrile episode during chemotherapy, the following data will be collected using a patient data form and computerized software.
Demographic data: age, gender, ethnicity. Clinical data: Underlying disease, immunizations, prophylactic antibiotics, presence of central venous catheter, intensity of chemotherapy, duration of fever, duration and severity of neutropenia, diagnosis of present event.
Imaging data Microbiological data Outcome The statistical analysis will be performed by an epidemiologist and statistician using the SPSS 12.0 software.
Detailed Description
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Conditions
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Keywords
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Hadassah Medical Organization
OTHER
Principal Investigators
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Dan Engelhard, MD
Role: PRINCIPAL_INVESTIGATOR
Hadassah Medical Organization
Diana Averbuch, MD
Role: PRINCIPAL_INVESTIGATOR
Hadassah Medical Organization
Central Contacts
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Other Identifiers
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yael12-HMO-CTIL
Identifier Type: -
Identifier Source: org_study_id