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

NARecruitingINTERVENTIONAL
Enrollment

120

Participants

Timeline

Start Date

September 25, 2020

Primary Completion Date

June 30, 2025

Study Completion Date

November 30, 2025

Conditions
Benign Prostatic HyperplasiaProstate HyperplasiaProstate DiseaseProstate HypertrophyProstate PainLower Urinary Tract SymptomsUrinary ObstructionUrinary Tract Disease
Interventions
DRUG

Finasteride

Patients who are candidates to receive 5ARI therapy, Finasteride, for clinical medical management of lower urinary tract symptoms will begin treatment once deemed eligible. They will be assess every 6 months for changes in urinary symptom scores and their responsiveness to the Finasteride treatment will be assessed at the 12-month time point. MRIs of prostate taken at the start of study and at the 3 year time point will assess prostate size and changes in size as well as degree of inflammatory changes. Gene expression of SRD5A2 as well as methylation pattern will be tested on prostate tissue samples, where hormonal androgen/estrogen levels will also be assessed as they are in blood samples.

Trial Locations (1)

02215

RECRUITING

Beth Israel Deaconess Medical Center, Boston

All Listed Sponsors
collaborator

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

NIH

lead

Beth Israel Deaconess Medical Center

OTHER