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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00660244
Other study ID # NIS-OAT-ARI-2007/1
Secondary ID
Status Completed
Phase N/A
First received April 15, 2008
Last updated June 5, 2012
Start date February 2008
Est. completion date December 2009

Study information

Verified date June 2012
Source AstraZeneca
Contact n/a
Is FDA regulated No
Health authority Austria: Agency for Health and Food Safety
Study type Observational

Clinical Trial Summary

The purpose of this study is to investigate efficacy and tolerability under anastrozole (Arimidex) treatment.


Recruitment information / eligibility

Status Completed
Enrollment 150
Est. completion date December 2009
Est. primary completion date
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- Postmenopausal women

- Already on upfront Arimidex Therapy (Start 1-4 weeks before)

- HR+

Exclusion Criteria:

- Premenopausal women

- Tamoxifen switch patients

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Drug:
anastrozole
Oral

Locations

Country Name City State
Austria Research Site Graz

Sponsors (1)

Lead Sponsor Collaborator
AstraZeneca

Country where clinical trial is conducted

Austria, 

Outcome

Type Measure Description Time frame Safety issue
Primary Progression of disease and tolerability in general Baseline, every 3 month No
Secondary Patient questionnaire to collect data on Incidence, time of onset and treatment of arthralgia Baseline, every 3 month No
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