Expired Study
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Portland, Oregon 97266


Purpose:

This project compares the Neusidl Corneal Injector (NCI) device developed by Fischer Surgical, Inc. for the delivery of tissue into the eye in DSAEK surgery to the current standard forceps insertion DSAEK technique. The goal of this study is to examine the damage to the corneal endothelium resulting from the use of the NCI device in comparison to the use of our standard surgical DSAEK technique over time.


Criteria:

Inclusion Criteria: - Age 21 and over - A diagnosis of Fuchs' Corneal Endothelial Dystrophy Exclusion Criteria: - Under age 21 - Diagnosis of advanced glaucomatous disease - Diagnosis of significant retinal disease - Diagnosis of any other corneal dystrophy - Previous corneal transplant surgery - Previous glaucoma surgery - Previous retinal surgery - Previous refractive surgery


NCT ID:

NCT01357122


Primary Contact:

Principal Investigator
Mark A Terry, MD
Devers Eye Institute


Backup Contact:

N/A


Location Contact:

Portland, Oregon 97266
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

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