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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01081509
Other study ID # NIS-OHU-ARI-2010/1
Secondary ID
Status Completed
Phase N/A
First received March 4, 2010
Last updated November 15, 2011
Start date March 2010
Est. completion date October 2011

Study information

Verified date November 2011
Source AstraZeneca
Contact n/a
Is FDA regulated No
Health authority Hungary: National Institute of Pharmacy
Study type Observational

Clinical Trial Summary

The aim of this study is to assess the patient's perception about and willingness to take his or her medication and the influencing factors interfering with taking medication.


Recruitment information / eligibility

Status Completed
Enrollment 1077
Est. completion date October 2011
Est. primary completion date October 2011
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria:

- Early breast cancer

- Post menopausal

- Adjuvant hormonal Arimidex therapy

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Hungary Research Site Balatonfoldvar
Hungary Research Site Bekescsaba
Hungary Research Site Budapest
Hungary Research Site Debrecen
Hungary Research Site Dombovar
Hungary Research Site Gyongyos
Hungary Research Site Gyor
Hungary Research Site Gyula
Hungary Research Site Kaposvar
Hungary Research Site Kecskemet
Hungary Research Site Miskolc
Hungary Research Site Mosdos
Hungary Research Site Nagyatad
Hungary Research Site Nyiregyhaza
Hungary Research Site Orfu
Hungary Research Site Papa
Hungary Research Site Pecs
Hungary Research Site Szeged
Hungary Research Site Szekesfehervar
Hungary Research Site Szekszard
Hungary Research Site Szentes
Hungary Research Site Szombathely
Hungary Research Site Veszprem
Hungary Research Site Zalaegerszeg
Hungary Research Site Zirc

Sponsors (1)

Lead Sponsor Collaborator
AstraZeneca

Country where clinical trial is conducted

Hungary, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percent of patients remaining adherent to therapy with Arimidex Every 3 months No
Secondary Questionnaire for factors influencing adherence Every 3 months No
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