Study identifier:D0816R00004
ClinicalTrials.gov identifier:NCT02262273
EudraCT identifier:N/A
CTIS identifier:N/A
Real-World Treatment Patterns, BRCA Testing Practices, Outcomes, and Health Care Utilization in Platinum-Sensitive Recurrent Serous Ovarian Cancer: A Multi-Country Retrospective Study
platinum-sensitive recurrent serous ovarian cancer
N/A
No
-
Female
2123
Observational
18 Years +
Allocation: N/A
Endpoint Classification: -
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: -
Verified 01 Feb 2017 by AstraZeneca
AstraZeneca
RTI Health Solutions, A+A Healthcare Marketing Research, Freelance CRA (FCRA)
This study will be carried out as a retrospective, non-interventional observational review of medical records for patients in multiple countries with platinum-sensitive recurrent serous ovarian cancer. The objectives are to describe in a real-world population, treatment patterns, BRCA mutation testing and results, overall survival, health care utilization and also to estimate rates of selected treatment- and/or disease-related side effects
Location
Location
London, United Kingdom
Location
Manchester, United Kingdom
Location
Leeds, United Kingdom
Location
Oxford, United Kingdom
Location
Brighton, United Kingdom
Location
Basingstoke, United Kingdom
Location
Bradford, United Kingdom
Location
Bristol, United Kingdom
Arms | Assigned Interventions |
---|---|
Serous ovarian cancer: Women with platinum-sensitive recurrent serous ovarian cancer | Other: Data Collection Colleciton of data from medical records only |
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