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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RECRUITING
8000 participants
OBSERVATIONAL
2014-12-01
2034-12-31
Brief Summary
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Detailed Description
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Data relating to the clinical conditions (state of the disease, psychological and related to the quality of life) of patients suffering from BPH under medical therapy and/or undergoing surgery will be collected within a specially designed database which will allow us to easily and secure extraction of data used for statistical analyzes in clinical research.
Conditions
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Keywords
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Patients with a benign prostatic hyperplasia condition
Patients with a benign prostatic hyperplasia condition
Observation of patients with a benign prostatic hyperplasia condition
Observation of patients with a benign prostatic hyperplasia condition who have undergone surgery
Interventions
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Observation of patients with a benign prostatic hyperplasia condition
Observation of patients with a benign prostatic hyperplasia condition who have undergone surgery
Eligibility Criteria
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Inclusion Criteria
* subjects \>= 18 years old
* signature of informed consent
Exclusion Criteria
* presence of mental or physical disability that may prevent the patient from answering the questionnaires.
18 Years
MALE
No
Sponsors
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IRCCS San Raffaele
OTHER
Responsible Party
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Andrea Salonia
Professor
Principal Investigators
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Andrea Salonia, MD
Role: PRINCIPAL_INVESTIGATOR
IRCCS Ospedale San Raffaele
Locations
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IRCCS Ospedale San Raffaele
Milan, Lombardy, Italy
Countries
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Central Contacts
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Facility Contacts
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Alessia d'Arma, MSc
Role: primary
Other Identifiers
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2014 - IPB
Identifier Type: -
Identifier Source: org_study_id