EndoPAT Device for Endothelial Dysfunction in ED

Recruiting N/A Interventional Study
Erectile Dysfunction Hypogonadism, Male Endothelial Dysfunction
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Male
Study type
Interventional
Purpose
Diagnostic
Participants needed
120 (estimated)
Sponsor
University of California, Irvine · Other
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About This Trial
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 testoste…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Males 18 years old and above * Diagnosed with erectile dysfunction or hypogonadism Exclusion Criteria: * Patients without the above criteria
Contacts

Muhammed AM Hammad, MBBCh

714-456-7005

mahammad@hs.uci.edu

CONTACT

Elia Abou Chawareb, MD

714-456-7005

eaboucha@hotmail.com

CONTACT