Prostatic Hyperplasia
Conditions
Interventions
This is an observational, prospective cohort study. A group of 30 patients with Benign Prostatic Hyperplasia with symptoms of the lower urinary tract followed at the Discipline of Urology, Department
N40.1
D08.811.277.656.300.760.442.750
Sponsors
Unifesp - Universidade Federal de São Paulo
Unifesp - Universidade Federal de São Paulo
Eligibility
Sex/Gender
Male
Age
18 Years to 90 Years
Inclusion criteria
Inclusion criteria: Men; age between 18 and 90 years; with benign prostatic hyperplasia; refractory to drug treatment; consistent with surgical treatment
Exclusion criteria
Exclusion criteria: patients who refuse to undergo magnetic resonance imaging and those with infectious processes or suspected prostate cancer on examination that causes an anatomical and structural deformity of the gland
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find a difference of more than 20% between the weight of the open transvesical prostatectomy surgical specimen and this same specimen after in vitro resection | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are not expected. | — |
Countries
Brazil
Contacts
Public ContactAndré Silva
Unifesp - Universidade Federal de São Paulo
Outcome results
None listed