5-Alpha Reductase 2 as a Marker of Resistance to 5ARI Therapy
Recruiting now · Not applicable
Conditions studied: Benign Prostatic Hyperplasia, Prostate Hyperplasia, Prostate Disease, Prostate Hypertrophy, Prostate Pain, Lower Urinary Tract Symptoms, Urinary Obstruction, Urinary Tract Disease
In brief
The study is being conducted to learn why some patients with Benign Prostatic Hyperplasia (BPH) do not respond to a commonly used treatment drug, Finasteride. The hope is to find ways to predict which patients will not respond to Finasteride so that, in the future, these patients can be identified prior to offering this treatment and they can be offered alternative treatment strategies in its place. The aim is to see if noninvasive techniques such as MRI can detect inflammation of the prostate to assist with early detection of those who will and who will not respond to Finasteride.
Key facts
- Study ID
- NCT04288427
- Run by
- Beth Israel Deaconess Medical Center
- People needed
- 120
- Starts
- 2020-09-25
- Expected to finish
- 2026-11-30
- Last updated by the study team
- 2025-10-28
Who can join
Age: 50 and older. Sex: male. Healthy volunteers: not accepted.
You may qualify if…
- Male (physiological);
- Age ≥ 50;
- Eligible for treatment with 5ARI therapy;
- Presence of lower urinary tract symptoms secondary to BPH;
- Prostate size >40cc by digital rectal examination;
- Absence of prostate nodule, tenderness or firmness;
- Mildly elevated PSA's >1.5 ng/ml and ≤ 40 ng/ml;
- Undergoing clinically indicated prostate biopsy for elevated prostate-specific antigen (PSA).
You may not qualify if…
- Diagnosis of any prostatic malignancy or precancerous lesions (atypical glandular foci and prostatic intraepithelial neoplasia);
- Treatment with 5ARI (Finasteride or Dutasteride) within six months of study enrollment;
- Current urinary tract infection;
- Previous pelvic radiation;
- Previous treatment with demethylating drugs;
- Diagnosis of multiple sclerosis, Alzheimer's, Parkinson's, neurological deficits in the judgment of the investigator;
- Unable or unwilling to undergo MRI due to implants, claustrophobia, etc.
Where it is running
- Beth Israel Deaconess Medical Center — Boston, Massachusetts, United States (enrolling)
Full record on ClinicalTrials.gov
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