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Clinical Trials/ISRCTN97879847
ISRCTN97879847CompletedNot Applicable

A study to determine the effect of post-infusion cooling time in the high dose 5-fluorouracil, 4-epidoxorubicin and cyclophosphamide (FEC)-regime

Medical Centre Alkmaar (Medisch Centrum Alkmaar) (The Netherlands)0 sites130 target enrollmentStarted: July 21, 2006Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
130

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Sex
Female

Inclusion Criteria

  • 1. Intravenously administered FEC-regimen with an epirubicin dose of 90 mg/m^2 or more at three-weekly intervals
  • 2. Aged 18 years or more
  • 3. Written informed consent

Exclusion Criteria

  • 1. Baldness before the start of the study
  • 2. Hematological malignancies with generalized haematogenic metastases and if in those conditions chemotherapy is given with a curative intent
  • 3. Clinical signs of scalp metastases

Investigators

Sponsor
Medical Centre Alkmaar (Medisch Centrum Alkmaar) (The Netherlands)

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