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RECRUITING
NCT06720597
NA

EndoPAT Device for Endothelial Dysfunction in ED

Sponsor: University of California, Irvine

View on ClinicalTrials.gov

Summary

To assess endothelial dysfunction in young men (aged 30-50) with vasculogenic ED identified through penile Doppler ultrasound. To evaluate changes in endothelial function using EndoPAT before and 3-6 months after daily low-dose phosphodiesterase type 5 (PDE5) inhibitor therapy. To investigate endothelial function alterations in hypogonadal patients before and 3-6 months after initiating testosterone (T) therapy

Official title: Utilizing EndoPAT Device for Endothelial Dysfunction Assessment in Erectile Dysfunction and Hormonal Therapy

Key Details

Gender

MALE

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

120

Start Date

2025-08-13

Completion Date

2027-01

Last Updated

2026-02-02

Healthy Volunteers

No

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.

Locations (1)

UCI Urology | Men's Health Center

Newport Beach, California, United States