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Muticentre study to investigate the efficacy of scalp cooling for the prevention of Myocet/cyclofosfamide-induced alopecia in patients with metastatic breast cancer. MyCap study

Completed
Conditions
haaruitval t.g.v. chemotherapie
alopecia
hair loss
Registration Number
NL-OMON35380
Lead Sponsor
Stichting DIADOC
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
70
Inclusion Criteria

* Female breast cancer patients, treated with Myocet and cyclophosphamide containing chemotherapy.
* Life expectancy * 12 weeks.
* ECOG performance scale * 2.
* Age 18 years and above.

Exclusion Criteria

* Allopecia prior to start of the study.
* Simultaneously or shortly after study start: planned skull irradiation (if allopecia is expected).
* Severely disturbed liver enzymes (see protocol for details).
* Hair extensions

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>Allopecia measured by trichometry.</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>Subjective severity of allopecia.</p><br>
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