- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00733213
Depiction of Prostate Cancer Treatment Alternatives in Greece
October 13, 2009 updated by: AstraZeneca
A retrospective, registry analysis of the socio-economic and demographic characteristics of patients suffering from locally advanced or metastatic prostate cancer, as well as the depiction of the therapeutic algorithms followed in the Greek clinical practice.
- Target Group: Patients with locally advanced or metastatic prostate cancer.
- The first 10 consecutive patients records that meet the entry criteria.
Study Overview
Status
Completed
Study Type
Observational
Enrollment (Anticipated)
310
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Athens, Greece
- Research Site
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Karditsa, Greece
- Research Site
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Serres, Greece
- Research Site
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Xsanthi, Greece
- Research Site
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Sampling Method
Probability Sample
Study Population
Target Group: Patients diagnosed with Locally advanced or Metastatic Prostate Cancer
Description
Inclusion Criteria:
- Patients diagnosed with Locally advanced or Metastatic Prostate Cancer after 2002.
- Patients that received Hormonal therapy.
Exclusion Criteria:
- Males that are aged less than 18 years
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Percentage of patients treated by each treatment alternative.
Time Frame: Between 2002 - 2008
|
Between 2002 - 2008
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
To depict sociodemographic characteristics and comorbidities.
Time Frame: Between 2002 - 2008
|
Between 2002 - 2008
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Panagiotis Pontikis, MD, AstraZeneca Greece
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2008
Study Completion (Actual)
March 1, 2009
Study Registration Dates
First Submitted
August 8, 2008
First Submitted That Met QC Criteria
August 11, 2008
First Posted (Estimate)
August 12, 2008
Study Record Updates
Last Update Posted (Estimate)
October 14, 2009
Last Update Submitted That Met QC Criteria
October 13, 2009
Last Verified
October 1, 2009
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- NIS-OGR-DUM-2007/1
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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