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Terminated Phase 4 Interventional Results available

PDE5 Inhibitor Use and Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)

ClinicalTrials.gov ID: NCT00867815

Public ClinicalTrials.gov record NCT00867815. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 25, 2026, 10:59 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Prospective Case Crossover Study to Assess Whether PDE5 Inhibitor Exposure in Men Increases the Risk for the Development of Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The primary objective of this study is to determine whether the use of PDE5 inhibitors (vardenafil, sildenafil, or tadalafil) increases the risk for the development of NAION.

Study identification

NCT ID
NCT00867815
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 4
Lead sponsor
Bayer
Industry
Enrollment
10 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 Years and older
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 13, 2009 (Actual)
Primary completion
Dec 29, 2017 (Actual)
Completion
Mar 28, 2018 (Actual)
Last update posted
Jan 23, 2019

2009 – 2018

United States locations

U.S. sites
11
U.S. states
8
U.S. cities
10
Facility City State ZIP Site status
Greider Eye Associates Vista California 92083 —
Palm Beach Eye Center Atlantis Florida 33461 —
West Coast Eye Care Fort Myers Florida 33908 —
National Ophthalmic Research Institute Fort Myers Florida 33912 —
Sarasota Retina Institute Sarasota Florida 34239 —
Midwest Eye Institute Indianapolis Indiana 46290 —
Spoor and Associates Warren Michigan 48088 —
Asheville Eye Associates Asheville North Carolina 28803 —
Office of Dr. Avrom Epstein, MD Columbus Ohio 43215-7312 —
Tulsa Clinical Research, LLC Tulsa Oklahoma 74014 —
Retinal and Ophthalmic Consultants Houston Texas 77030 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00867815, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 23, 2019 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00867815 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →