Quality of Life Analysis of Arimidex Treatment in Postmenopausal Patients With Breast Cancer

Overview

This is an open label, non-interventional quality of life analysis for Arimidex treated postmenopausal patients in early breast cancer by investigator's questionnaire

Study Type

  • Study Type: Observational
  • Study Design
    • Time Perspective: Prospective
  • Study Primary Completion Date: July 2010

Clinical Trial Outcome Measures

Primary Measures

  • Elements of the investigator questionnaire SF RAND-36 questionnaire
    • Time Frame: Quarterly (plus or minus 3 days )

Secondary Measures

  • Investigator Assessment Report
    • Time Frame: Yearly (plus or minus 1 week )

Participating in This Clinical Trial

Inclusion Criteria

  • Provision of informed consent – Postmenopausal, hormon receptor positive patients with early breast cancer treated with Arimidex – Investigators are requested to recruit patients only with at least 1 month prior Arimidex treatment. Exclusion Criteria:

  • Allergy to substance of medication – Pre-perimenopausal woman – Woman not eligible for treatment

Gender Eligibility: Female

Minimum Age: N/A

Maximum Age: N/A

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • AstraZeneca
  • Provider of Information About this Clinical Study
    • Sponsor
  • Overall Official(s)
    • Zsolt Horváth, M.D., Principal Investigator, National Institute of Oncology
    • Csaba Csongvai, Study Director, AstraZeneca Hungary
    • Éva Gulyás, Study Chair, AstraZeneca Hungary

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