Enhanced Clinical Decisions for Management of Benign Prostatic Hyperplasia Using Patient-Reported Outcomes

Recruiting Observational Study
Benign Prostatic Hyperplasia
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
50 and older
Sex
Male
Study type
Observational
Participants needed
300 (estimated)
Sponsor
Northwestern University · Other
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About This Trial
The goal of this project is to use newly developed patient-reported outcomes to improve the clinical care of patients with benign prostatic hyperplasia. The use of new patient-centered tools will improve evaluation and clinical decision-making by including symptoms not commonly measured in men, such as urinary incontinence, and allow for more frequent assessment of lower urinary tract symptoms thr…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Male sex 2. Age 50 years or older 3. Diagnosed by physician with BPH 4. Able and willing to complete questionnaires 5. Able and willing to provide informed consent 6. Ability to read, write, and speak in English 7. No plans to move from study area in next 6 months Exclusion …
Contacts

Dacey Maglaque

847-503-4278

dmaglaque2@northshore.org

CONTACT

Pooja Talaty

847-503-4280

PTalaty@northshore.org

CONTACT