EndoPAT Device for Endothelial Dysfunction in ED

NARecruitingINTERVENTIONAL
Enrollment

120

Participants

Timeline

Start Date

August 13, 2025

Primary Completion Date

January 31, 2027

Study Completion Date

January 31, 2027

Conditions
Erectile DysfunctionHypogonadism, MaleEndothelial Dysfunction
Interventions
DRUG

Daily low-dose PDE5 inhibitor therapy

Neither arm of the study includes a control group, and the two interventions will not be compared directly. The primary objective is to evaluate endothelial function using the EndoPAT device at baseline, 3 months, and 6 months following the intervention in each arm.

DRUG

Testosterone therapy as per clinical guidelines.

Neither arm of the study includes a control group, and the two interventions will not be compared directly. The primary objective is to evaluate endothelial function using the EndoPAT device at baseline, 3 months, and 6 months following the intervention.

Trial Locations (1)

California

RECRUITING

"UCI Urology , Men's Health Center"

All Listed Sponsors
lead

University of California, Irvine

OTHER

NCT06720597 - EndoPAT Device for Endothelial Dysfunction in ED | Biotech Hunter | Biotech Hunter