NCT03069521View on ClinicalTrials.gov

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

NACompletedINTERVENTIONAL
Enrollment

22

Participants

Timeline

Start Date

June 22, 2017

Primary Completion Date

January 30, 2023

Study Completion Date

January 30, 2023

Conditions
Chronic Cornel Edema
Interventions
DEVICE

EndoArt® Artificial Endothelial Layer

device is intended for use as an endothelial kearatoprosthesis

Trial Locations (8)

Unknown

International Vision Correction Research Centre (IVCRC) Universitätsklinikum Heidelberg, Heidelberg

Barzilai MC, Ashkelon

Soroka Medical Center, Beersheba

Rambam Medical Center, Haifa

Assuta Medical Center, Tel Aviv

Tel Aviv Souraski Medical Center, Tel Aviv

AMC, Amsterdam

IMO - Institut de Microcirurgia Ocular, Barcelona

Sponsors

Lead Sponsor

Eye-yon Medical
All Listed Sponsors
lead

Eye-yon Medical

INDUSTRY

NCT03069521 - Study to Evaluate the Safety of the EndoArt™ for Treatment of Subjects Suffering From Corneal Edema | Biotech Hunter | Biotech Hunter