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Survey in Post-menopausal Women Followed up After Treatment With Anastrozole as Adjuvant Therapy (ARIES)

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ClinicalTrials.gov Identifier: NCT00542594
Recruitment Status : Terminated (No results are avaialble as the study did not complete according to the protocol)
First Posted : October 11, 2007
Last Update Posted : February 7, 2013
Information provided by (Responsible Party):

Study Description
Brief Summary:
The purpose of this survey is to describe long-term tolerance as seen under current conditions of use for anastrozole.

Condition or disease
Breast Cancer

Study Design

Study Type : Observational
Actual Enrollment : 1840 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: A Report Upon a Cohort of Post-menopausal Women Followed up After Treatment With Anastrozole as Adjuvant Therapy for Hormone-dependant Breast Cancer. Long-term Tolerance Evaluation
Study Start Date : November 2005
Primary Completion Date : June 2011
Study Completion Date : June 2011

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Breast Cancer
Drug Information available for: Anastrozole
U.S. FDA Resources

Groups and Cohorts

Outcome Measures

Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Woman seen by their physician in the current care setting and for whom a treatment with anastrozole is decided by the physician (adjuvant treatment of breast cancer in postmenopausal women with hormone receptor positive status)

Inclusion Criteria:

  • woman treated with anastrozole as adjuvant therapy for hormone-dependant breast cancer in post-menopausal women with positive hormone-receptors
Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00542594

Sponsors and Collaborators
Study Director: AstraZeneca France Medical Director AstraZeneca
More Information

Responsible Party: AstraZeneca
ClinicalTrials.gov Identifier: NCT00542594     History of Changes
Other Study ID Numbers: NIS-OFR-ARI-2005/1
First Posted: October 11, 2007    Key Record Dates
Last Update Posted: February 7, 2013
Last Verified: February 2013

Keywords provided by AstraZeneca:
breast cancer

Additional relevant MeSH terms:
Breast Neoplasms
Neoplasms by Site
Breast Diseases
Skin Diseases
Antineoplastic Agents, Hormonal
Antineoplastic Agents
Aromatase Inhibitors
Steroid Synthesis Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action
Estrogen Antagonists
Hormone Antagonists
Hormones, Hormone Substitutes, and Hormone Antagonists
Physiological Effects of Drugs