Effectiveness of an N-acetylcysteine and Urea-based Cream in Prevention of Capecitabine-induced HAND-foot Syndrome in Breast Cancer Patients

Recruiting N/A Interventional Study
Breast Cancer
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Prevention
Participants needed
25 (estimated)
Sponsor
Centro di Riferimento Oncologico - Aviano · Other
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About This Trial
Breast cancer (BC) is the most frequent tumour in women. To date, among the available treatments, the use of Capecitabine, an oral prodrug of fluorouracil, has been shown activity in different setting. In advanced disease, Capecitabine is often used as monotherapy in patients pretreated with anthracycline, taxane or both. One of the most frequent toxicities reported by patients receiving capecita…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Women and men ≥18 years old * Patients with diagnosis of breast cancer with stage I-III radically operated with residual disease post neoadjuvant treatment or stage IV * Patients candidated for capecitabine in a post-neoadjuvant or metastatic setting treated with 2000-2500 mg/…
Contacts

Simon Spazzapan, MD

+39 0434 659725

spazzapan@cro.it

CONTACT