Electronic Study for Anastrozole Pharmacovigilance Evaluation
E-SAFE
1 other identifier
observational
1,850
0 countries
N/A
Brief Summary
Collecting information regarding adverse events from patients on treatment with anastrazole with early stage breast cancer
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2004
Longer than P75 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2004
CompletedFirst Submitted
Initial submission to the registry
November 13, 2007
CompletedFirst Posted
Study publicly available on registry
November 14, 2007
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2008
CompletedJuly 28, 2008
July 1, 2008
November 13, 2007
July 25, 2008
Conditions
Keywords
Eligibility Criteria
You may qualify if:
- Post-menopausal Early Invasive Breast Cancer Patients who are under anastrazole treatment, who have normal renal and hepatic functions.
You may not qualify if:
- Metastatic breast cancer patients, previous hormonal therapy, other malignancies.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- AstraZenecalead
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Nejdet Uskent
Kadir Has University Medical School
Study Design
- Study Type
- observational
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- INDUSTRY
Study Record Dates
First Submitted
November 13, 2007
First Posted
November 14, 2007
Study Start
January 1, 2004
Study Completion
July 1, 2008
Last Updated
July 28, 2008
Record last verified: 2008-07