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Spots Global Cancer Trial Database for F511 Cream in Preventing Palmar-Plantar Erythrodysesthesia in Patients Receiving Doxorubicin Hydrochloride Liposome for Metastatic Breast Cancer

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Trial Identification

Brief Title: F511 Cream in Preventing Palmar-Plantar Erythrodysesthesia in Patients Receiving Doxorubicin Hydrochloride Liposome for Metastatic Breast Cancer

Official Title: Local Antiperspirant for Prevention of Palmar-Plantar Erythrodysesthesia (PPE) in Patients Treated With Pegylated Liposomal Doxorubicin: A Randomized, Multicenter, Double Blinded, Phase III Trial

Study ID: NCT00992706

Study Description

Brief Summary: RATIONALE: F511 cream may prevent or reduce palmar-plantar erythrodysesthesia in women receiving doxorubicin hydrochloride liposome for metastatic breast cancer. PURPOSE: This randomized phase III trial is studying F511 cream to see how well it works compared with a placebo cream in preventing palmar-plantar erythrodysesthesia in patients receiving doxorubicin hydrochloride liposome for metastatic breast cancer.

Detailed Description: OBJECTIVES: * Evaluate the effects of F511 cream on the occurrence of palmar-plantar erythrodysesthesia (PPE) in patients with metastatic breast cancer treated with pegylated liposomal doxorubicin hydrochloride. OUTLINE: This is a multicenter study. Patients receive pegylated liposomal doxorubicin hydrochloride according to local practice on 1, 2, or 4 weeks course schedules with at least 10 mg/m\^2 per week allowed. Patients apply F511 cream on one side, hand and foot and the corresponding placebo on the other side hand and foot once daily (the morning) during the first week of the first pegylated liposomal doxorubicin hydrochloride treatment only, then once daily, three times per week thereafter. Treatment continues throughout chemotherapy administration in the absence of palmar-plantar erythrodysesthesia (PPE) ≥ grade 2 After completion of study therapy, patients are followed for 30 days. Patients with PPE ≥ grade 2 are followed until the PPE resolves to ≤ grade 1.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Kantonsspital Aarau, Aarau, , Switzerland

Kantonsspital Baden, Baden, , Switzerland

Universitaetsspital-Basel, Basel, , Switzerland

Spitalzentrum Biel, Biel, , Switzerland

Spital Buelach, Bulach, , Switzerland

Kantonsspital Graubuenden, Chur, , Switzerland

Hopital Cantonal Universitaire de Geneve, Geneva, , Switzerland

Centre Hospitalier Universitaire Vaudois, Lausanne, , Switzerland

Kantonsspital Luzern, Luzerne, , Switzerland

Kantonsspital Olten, Olten, , Switzerland

Onkologie Schaffhausen, Schaffhausen, , Switzerland

Institut Central des Hopitaux Valaisans, Sion, , Switzerland

Kantonsspital - St. Gallen, St. Gallen, , Switzerland

Kantonsspital Winterthur, Winterthur, , Switzerland

UniversitaetsSpital Zuerich, Zurich, , Switzerland

Contact Details

Name: Thomas Ruhstaller, MD

Affiliation: Cantonal Hospital of St. Gallen

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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