Status:

COMPLETED

Distinction Risk of Severe Infection in Febrile Neutropenia After Chemotherapy

Lead Sponsor:

University Hospital, Lille

Collaborating Sponsors:

Ministry of Health, France

Ligue contre le cancer, France

Conditions:

Febrile Neutropenia, Rule of Clinical Decision, Chemotherapy

Eligibility:

All Genders

1-18 years

Brief Summary

Evaluate the reproducibility and validate a posteriori a new rule of clinical decision on a multi-center population of children with a post-chemotherapy febrile neutropenia

Eligibility Criteria

Inclusion

  • Child aged 1 to 18 years
  • Child with hematology or cancer
  • Child with a febrile neutropenia post-chemotherapy
  • Child with social security
  • No opposition from the child and/or parents, in case of absence, the holder of the parental authority present, can consent, alone, to the participation of the unemancipated minor.

Exclusion

  • Febrile neutropenia at diagnosis of tumor disease
  • Child with palliative care
  • Child having had a hematopoietic stem cell allo-graft in the preceding year
  • Febrile neutropenia immediately post auto-transplant
  • Antibiotherapy prior to admission
  • Initial care in a non-investigative center.

Key Trial Info

Start Date :

May 1 2012

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

May 1 2017

Estimated Enrollment :

1900 Patients enrolled

Trial Details

Trial ID

NCT03434795

Start Date

May 1 2012

End Date

May 1 2017

Last Update

February 15 2018

Active Locations (1)

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Hôpital Jeanne de Flandre - CHRU de Lille

Lille, France