Active Surveillance for Prostate Cancer With Indolent Features
NCT ID: NCT00421265
Last Updated: 2007-01-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
150 participants
OBSERVATIONAL
Brief Summary
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Detailed Description
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Conditions
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Study Design
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DEFINED_POPULATION
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
2. Gleason's score of 6 or less.
3. Clinical T1C per digital rectal exam.
4. Pre biopsy PSA serum level of 6.0ng/ml or less.
5. The presence of cancer in a single biopsy core of at least 8 taken.
6. The presence of cancer in no more than 10% of the length of the core involved.
7. Patient's consent to engage in active surveillance after being informed of the benefits and potential risks of this approach as well as of alternative lines of therapy.
8. Israeli residence with the readiness to be available for the followup schedule.
Exclusion Criteria
65 Years
80 Years
MALE
No
Sponsors
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Assaf-Harofeh Medical Center
OTHER_GOV
Principal Investigators
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Dan Leibovici, M.D.
Role: PRINCIPAL_INVESTIGATOR
Assaf-Harofeh Medical Center
Locations
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Assaf Harofeh Medical Center
Ẕerifin, , Israel
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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138/06
Identifier Type: -
Identifier Source: org_study_id
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