NCT03069521

Study to Evaluate the Safety of the EndoArt™ for Treatment of Subjects Suffering From Corneal Edema

Prospective, Feasibility Study to Evaluate the Safety of the EndoArt™ for Treatment of Subjects Suffering From Corneal Edema

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 22 (actual)
• Sponsor: Eye-yon Medical · Industry
• Sex: All
• Age: 40 Years
• Healthy volunteers: Not accepted

Summary

Prospective, feasibility study to evaluate the safety of the EndoArt® for treatment of 30 subjects suffering from corneal edema. Followed up for 12 months.

Detailed description

Title: Prospective, feasibility study to evaluate the safety of the EndoArt® for treatment of subjects suffering from corneal edema Device: EndoArt® (Artificial Endothelial Layer) Intended Use: The EndoArt® device is intended for use as an endothelial kearatoprosthesis in patients with chronic cornel edema Study Design: Prospective open-label feasibility clinical study Study Objectives: To evaluate the safety of the EndoArt® implanted in subjects suffering from corneal edema. Study Hypothesis: Treatment with the EndoArt® is safe and may result in alleviating symptoms resulting from chronic corneal edema (corneal thickness). Study population: Men and women suffering from a decrease in vision due to chronic corneal edema that meet the inclusion/exclusion criteria and provide written Informed Consent will enrolled in the study. Enrollment: A total of up to 30 subjects will be enrolled. Study Duration: Completion of active enrollment is anticipated to last approximately 18 months. The primary end point will be achieved when the final study subject has completed 6 month follow up. Subject will be followed up to 12 month. Primary Safety Endpoint: The frequency and severity of all treatment-related adverse events, during and after implantation of the EndoArt® and throughout the 6 month follow-up period. Adverse events will be assessed on a continuous basis from the procedure through the study completion at 6 months. Related adverse events include: corneal perforation, melting, uncontrolled inflammation, severe infection. Secondary Efficacy Endpoints: Corneal thickness, Subjective corneal clarity, Pain as assessed by a Visual Analogue Scale (VAS) Measurement Best Corrected Distance Visual Acuity (BCDVA) Study Treatment: Subjects will be implanted with the EndoArt®

Conditions

• Chronic Cornel Edema

Interventions

Type	Name	Description
DEVICE	EndoArt® Artificial Endothelial Layer	device is intended for use as an endothelial kearatoprosthesis

Timeline

• Start date: 2017-06-22
• Primary completion: 2023-01-30
• Completion: 2023-01-30
• First posted: 2017-03-03
• Last updated: 2023-02-16

Locations

8 sites across 4 countries: Germany, Israel, Netherlands, Spain