5-Alpha Reductase 2 as a Marker of Resistance to 5ARI Therapy

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexMale
Age50+
SponsorBeth Israel Deaconess Medical Center

About this trial

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.

Eligibility criteria

Qualifiers

Male (physiological);

Age ≥ 50;

Eligible for treatment with 5ARI therapy;

Presence of lower urinary tract symptoms secondary to BPH;

Disqualifiers

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;

Trial design

Treatments tested in this trial

  • Finasteride

Treatment groups

120 Participants
are divided into 1 treatment group

Sponsors and collaborators

Beth Israel Deaconess Medical Center

Lead sponsor

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Collaborator