Status:

COMPLETED

Observational Non-Interventional Study Of Febrile Neutropenia Patients To Evaluate Antibacterial Therapeutical Options

Lead Sponsor:

Pfizer

Conditions:

Febrile Neutropenia

Eligibility:

All Genders

18+ years

Brief Summary

The purpose of this study was to define and classify antibacterial agents used in Turkey for patients with febrile neutropenia.

Eligibility Criteria

Inclusion

  • Patients who are 18 years old and above.
  • Patients who have undergone allogeneic/autologous or peripheral stem cell transplantation following induction or consolidation treatment due to acute hematological malignancy.
  • Patients who have a neutrophil count below 500 cells per cubic millimeter (cells/mm\^3) or below 1000 cells/mm\^3 with an expectancy to rapidly decrease below 500 cells/mm\^3.
  • Patients with a body temperature more than or equal to (≥)38.3 degrees Celsius (101 degrees Fahrenheit) on single oral measurement or detected ≥38.0 degrees Celsius for at least an hour and thus started on antibacterial treatment will be included in the trial.

Exclusion

  • \- Patients who are pregnant or considering pregnancy.

Key Trial Info

Start Date :

June 1 2009

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

October 1 2010

Estimated Enrollment :

264 Patients enrolled

Trial Details

Trial ID

NCT00945555

Start Date

June 1 2009

End Date

October 1 2010

Last Update

April 5 2017

Active Locations (5)

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Page 1 of 2 (5 locations)

1

Pfizer Investigational Site

Kayseri, Turkey, Turkey (Türkiye)

2

Pfizer Investigational Site

Kocaeli, Turkey, Turkey (Türkiye)

3

Pfizer Investigational Site

Ankara, Turkey (Türkiye), 06500

4

Pfizer Investigational Site

Bursa, Turkey (Türkiye)