Clinical Trials Directory

Trials / Unknown

UnknownNCT01658956

Effectiveness of Reduced GCSF Dosing in Patients With a Low to Moderate Risk of Febrile Neutropenia

A Phase II Randomized Study to Verify the Papaldo's Hypothesis : the Effectiveness of a Reduced Dosing of G-CSF in Chemotherapy-treated Patients With a Low to Moderate Risk of Febrile Neutropenia

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
142 (estimated)
Sponsor
Jules Bordet Institute · Academic / Other
Sex
Female
Age
Healthy volunteers
Not accepted

Summary

The study aims to confirm that a reduced dosage of GCSF is effective in preventing febrile neutropenia among patients with breast cancer, treated with chemotherapy and presenting with a low to moderate risk of developing febrile neutropenia.

Conditions

Interventions

TypeNameDescription
DRUGGCSF administration on days 8 and 12 after chemotherapy

Timeline

Start date
2012-07-01
Primary completion
2015-07-01
Completion
2015-07-01
First posted
2012-08-07
Last updated
2015-01-06

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT01658956. Inclusion in this directory is not an endorsement.

Effectiveness of Reduced GCSF Dosing in Patients With a Low to Moderate Risk of Febrile Neutropenia (NCT01658956) · Clinical Trials Directory