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A Prospective Case-crossover Study to Evaluate the Possible Association Between the Use of PDE5 Inhibitors and the Risk of Acute Nonarteritic Anterior Ischemic Optic Neuropathy (NAION)

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City:   Chattanooga
State:   Tennessee
Zip Code:   37421
Conditions:   Nonarteritic Anterior Ischemic Optic Neuropathy
Purpose:   Study H6D-MC-LVHQ is an observational, non-interventional, multi-center, prospective, case-crossover study to evaluate the possible association between the use of phosphodiesterase type 5 (PDE5) inhibitors and the risk of acute nonarteritic anterior ischemic optic neuropathy (NAION) in males. Subjects with newly diagnosed NAION will be asked via a structured questionnaire about their use of PDE5 inhibitors and other risk factors prior to the onset of their vision loss.
Study Summary:  
Criteria:   Inclusion Criteria: - Adult male subjects, at least 18 years of age, who are willing to participate in the study - Patients who experienced abrupt visual loss in one eye (defined as typically less than a 1-day period or visual loss noted upon awakening) and presented for an initial visit within 45 days of onset of NAION symptoms to an ophthalmologist that resulted in a diagnosis of Suspected NAION by the investigator Exclusion Criteria: - Previous history of NAION - Previous history of arteritis (anywhere in the body) or clinical or diagnostic testing evidence of temporal arteritis - History of glaucoma in either one or both eyes - History of multiple sclerosis or diagnostic testing evidence of optic neuritis - Have dementia or other reasons for memory impairment in the opinion of the investigator - Have participated in other non-observational studies within 3 months of NAION onset
NCT ID:   NCT01131104
Primary Contact:   Study Director
Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon-Fr- 9 AM-5 PM Eastern time (UTC?GMT - 5 hours, EST)
Eli Lilly and Company

There may be multiple sites in this observational study 1-877-CTLILLY (1-877-285-4559)
Phone: 317-615-4559
Backup Contact:   N/A
Location Contact:   Chattanooga, Tennessee 37421
United States

Eli Lilly

Site Status: Recruiting

Data Source:   ClinicalTrials.gov
Date Processed:   May 22, 2013
Modifications to this listing:   Only selected fields are shown, please use the link below to view all information about this clinical trial.
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