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Clinical Trial Summary

Study objective is to evaluate the initial safety and effectiveness of the GORE Synthetic Cornea Device in the treatment of loss of corneal clarity in patients who are candidates for corneal transplantation


Clinical Trial Description

This is a prospective, single-arm, open-label, multi-center early feasibility clinical study designed to evaluate the clinical outcomes of the GORE Synthetic Cornea Device in the treatment of loss of corneal clarity in patients who are candidates for corneal transplantation. Following procedure, clinical follow up will be scheduled over the course of the study duration (12 months). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06174376
Study type Interventional
Source W.L.Gore & Associates
Contact Anuraag Singh
Phone 410-506-7560
Email asingh@wlgore.com
Status Not yet recruiting
Phase N/A
Start date January 1, 2024
Completion date December 31, 2030

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