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Clinical Trial Summary

Recently, published literature has reported that performing a descemetorhexis in combination with topical Rho kinase (ROCK) inhibitor therapy was successful in clearing edematous corneas in patients with Fuchs Endothelial Corneal Dystrophy. Ripasudil hydrochloride hydrate( Glanatec ophthalmic solution 0.4%), a potent ROCK inhibitor, has been approved in Japan since 2014 for ocular use in the treatment of glaucoma. Ripasudil acts as an IOP-lowering drug by affecting aqueous outflow through the trabecular meshwork and Schlemm's canal. The goal of this study is to test the potential benefits of Ripasudil therapy administered after Descemet Membrane Endothelial Keratoplasty (DMEK) surgery. We believe that performing a standard DMEK surgery in combination with Ripasudil treatment in patients with Fuchs Endothelial Corneal Dystrophy could accelerate endothelial cell healing and clear edematous corneas faster, with less post-operative complications.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03813056
Study type Interventional
Source Legacy Health System
Contact Alex J Bauer, B.S.
Phone 503-413-8377
Email alex@visiongift.org
Status Recruiting
Phase Phase 2
Start date March 25, 2019
Completion date February 1, 2025

See also
  Status Clinical Trial Phase
Recruiting NCT02423213 - DISCOVER Study: Microscope-integrated Intraoperative OCT Study
Completed NCT00624221 - Study of Eye Bank Pre-cut Donor Grafts for Endothelial Keratoplasty N/A
Completed NCT04051463 - Rhopressa for Corneal Edema Associated With Fuchs Dystrophy Phase 2/Phase 3
Completed NCT02423161 - PIONEER: Intraoperative and Perioperative OCT Study N/A