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Trials / Completed

CompletedNCT01268878

Hematologic Toxicity Observation of the Docetaxel+ Cisplatin+ Fluorouracil (TPF)Medical Protocol

Hematologic Toxicity Observation of the TPF Medical Protocol. Description of the Impact of Febrile Neutropenia in Patients Who Receive the Chemotherapy of the TPF Medical Protocol in Head and Neck Cell Carcinoma

Status
Completed
Phase
Study type
Observational
Enrollment
130 (actual)
Sponsor
Groupe Oncologie Radiotherapie Tete et Cou · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The ending of this study is to describe the effect of febrile neutropenia on patients who receive a chemotherapy by docetaxel+cisplatin+fluorouracil(TPF).

Detailed description

In this study we will describe * habits of medical staff in prescription of growth factors or antibiotic prophylaxis * ratio of patients treated by growth factors in primary or secondary prophylaxis * ratio of patients treated in primary prophylaxis who present a febrile neutropenia * ratio of patients who need to be hospitalized and the duration of those hospitalizations. * causes of lateness, of decreasing, and of stop of chemotherapy * antibiotic and growth factors prophylaxis tolerance .

Conditions

Timeline

Start date
2010-06-01
Primary completion
2011-11-01
Completion
2011-11-01
First posted
2010-12-31
Last updated
2014-01-03

Locations

18 sites across 1 country: France

Source: ClinicalTrials.gov record NCT01268878. Inclusion in this directory is not an endorsement.

Hematologic Toxicity Observation of the Docetaxel+ Cisplatin+ Fluorouracil (TPF)Medical Protocol (NCT01268878) · Clinical Trials Directory