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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01715155
Other study ID # NIS-OBG-XXX-2012/1
Secondary ID
Status Completed
Phase N/A
First received October 22, 2012
Last updated August 21, 2013
Start date December 2012
Est. completion date June 2013

Study information

Verified date August 2013
Source AstraZeneca
Contact n/a
Is FDA regulated No
Health authority Bulgaria: Bulgarian Drug Agency
Study type Observational

Clinical Trial Summary

The purpose of this study is to evaluate the incidence rate of progression of disease, to describe the diagnostic and clinical management in patients with Metastatic Breast Cancer in the clinical practice in Bulgaria.


Description:

A Retrospective Cohort Study on Therapeutic Management of Metastatic Breast Cancer in Clinical Practice in Bulgaria


Recruitment information / eligibility

Status Completed
Enrollment 171
Est. completion date June 2013
Est. primary completion date June 2013
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- New diagnosis of breast cancer according to ICD-10 with confirmed metastasis

- Confirmed diagnosis between 1st July 2010 and 30th June 2011.

- Female patient managed for her disease at the same setting where final diagnosis of MBC was performed.

Exclusion Criteria:

- History of concurrent or other primary malignancies (except curatively resected non-melanoma skin cancer or in situ cervical cancer).

Study Design

Observational Model: Cohort, Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
Bulgaria Research Site Pleven
Bulgaria Research Site Plovdiv
Bulgaria Research Site Ruse
Bulgaria Research Site Sofia
Bulgaria Research Site Stara Zagora
Bulgaria Reaseach Site Varna

Sponsors (1)

Lead Sponsor Collaborator
AstraZeneca

Country where clinical trial is conducted

Bulgaria, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of progression events on a per patient-year-basis Up to 2 years 5 months No
Secondary Proportion of patients among study population who have not progressed at 12 and 18 months after they were diagnosed Up to 2 years 5 months No
Secondary Median and mean time interval that elapsed between diagnosis and first objective tumor progression (TTP) event and subsequent events Up to 2 years 5 months No
Secondary Median and mean time from the date of diagnosis to the date of breast cancer progression or death whichever occurred first Up to 2 years 5 months No
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