Home › Enlarged Prostate (BPH) › NCT05898932
Enhanced Clinical Decisions for Management of Benign Prostatic Hyperplasia Using Patient-Reported Outcomes
Who can join
Ages 50 and older · Men
Full 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 Criteria: 1. Female sex or intersex 2. Younger than 50 years of age 3. Being a prisoner or detainee 4. Gross hematuria 5. Interstitial cystitis 6. Pelvic or endoscopic genitourinary surgery within the preceding 6 months (not including diagnostic cystoscopy) 7. History of cystitis caused by tuberculosis, radiation therapy, or Cytoxan/cyclophosphamide therapy 8. Ongoing symptomatic urethral stricture 9. Current chemotherapy or other cancer therapy 10. History of lower urinary tract or pelvic malignancy 11. Severe neurological of psychiatric disorder that would prevent study participation (e.g., bipolar disorder, psychotic disorder, Alzheimer's Disease) 12. Current moderate or severe substance use disorder
About the study
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 through remote surveillance. Through the use of care-coordination checklists, clinicians can be more responsive to post-treatment symptom changes, resulting in reduced bother from lower urinary tract symptoms and higher quality of life in patients with benign prostatic hyperplasia.
What is being tested
- Medical Management (other)
- Surgical Management (other)
Sponsor: Northwestern University · Participants: 300 · Started: Jun 1, 2023
Contact the study team
- Dacey Maglaque · Phone: 847-503-4278
- Pooja Talaty · Phone: 847-503-4280
Official record on ClinicalTrials.gov — NCT05898932
Locations in the U.S.
| Illinois | Endeavor Health, Glenview |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.