Clinical Outcomes of the Gore Synthetic Cornea Device

Status Not yet recruiting

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

Corneal Opacity

Clinical Trial Details

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	July 1, 2024
Completion date	December 31, 2030

View Details

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