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

NCT03069521 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 22

Last updated 2023-02-16

No results posted yet for this study

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.

Conditions

  • Chronic Cornel Edema

Interventions

DEVICE

EndoArt® Artificial Endothelial Layer

device is intended for use as an endothelial kearatoprosthesis

Sponsors & Collaborators

  • Eye-yon Medical

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
40 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-06-22
Primary Completion
2023-01-30
Completion
2023-01-30

Countries

  • Germany
  • Israel
  • Netherlands
  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03069521 on ClinicalTrials.gov