RECRUITING

EndoPAT Device for Endothelial Dysfunction in ED

Description

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

Study Overview

Study Details

Study overview

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

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

EndoPAT Device for Endothelial Dysfunction in ED

Condition
Erectile Dysfunction
Intervention / Treatment

-

Contacts and Locations

Newport Beach

UCI Urology | Men's Health Center, Newport Beach, California, United States, 92660

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Males 18 years old and above
  • * Diagnosed with erectile dysfunction or hypogonadism
  • * Patients without the above criteria

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

MALE

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of California, Irvine,

Faysal A Yafi, MD, PRINCIPAL_INVESTIGATOR, University of California, Irvine

Study Record Dates

2027-01