Archive Prostate. Observational Study of Patients Who Underwent Radical Prostatectomy Surgery
NCT ID: NCT06154499
Last Updated: 2023-12-04
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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ACTIVE_NOT_RECRUITING
1784 participants
OBSERVATIONAL
2004-04-08
2025-02-13
Brief Summary
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Detailed Description
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Anamnesis, surgery, histological report and hospitalization data are collected for patients who underwent radical prostatectomy.
Each patient will be followed for 10 years from the date of radical prostatectomy surgery.
Each patient will receive a questionnaire before radical prostatectomy in order to evaluate the quality of life (urinary continence, erectile function and psycho-physical wellbeing). A follow up questionnaire will be collected after surgery in order to analyze the predictive factors of the disease, clinical progression and to obtain health benefits for the patients involved and for future patients with the same tipe of cancer, improving the scientific knowledge of the pathology and implementing new strategies for diagnosis and therapy and evaluating the epidemiologic changes of prostate cancer. Tha data collected will be handles following the most strict Good Clinical Practice (GCPs) and privacy norms.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Patients referred to the Urology Department who need to undergo radical prostatectomy surgery
Radical prostatectomy
Radical Prostatectomy: surgery to remove the prostate gland and seminal vesicles (and sometimes nearby lymph nodes) after a prostate cancer diagnosis
Interventions
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Radical prostatectomy
Radical Prostatectomy: surgery to remove the prostate gland and seminal vesicles (and sometimes nearby lymph nodes) after a prostate cancer diagnosis
Eligibility Criteria
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Inclusion Criteria
* Adult patients \> 18 years
* Ability to read and sign the informed consent
Exclusion Criteria
* mental or physical disability that may prevent the patient from satisfying the requirements of the protocol
* Inability to read and sign the informed consent
18 Years
MALE
No
Sponsors
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IRCCS San Raffaele
OTHER
Responsible Party
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Francesco Montorsi
Professor
Locations
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Francesco Montorsi
Milan, , Italy
Countries
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Other Identifiers
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2004- Prostata
Identifier Type: -
Identifier Source: org_study_id