A Phase II, Interventional, Double-blind, Single-center Study of the Effects of Ripasudil on Cornea Clearing After Descemet Membrane Endothelial Keratoplasty in Subjects With Fuchs' Endothelial Corneal Dystrophy

Who is this study for? Patients with Fuchs' endothelial corneal dystrophy
Status: Recruiting
Location: See location...
Intervention Type: Drug, Procedure
Study Type: Interventional
Study Phase: Phase 2
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 30
Maximum Age: 99
Healthy Volunteers: f
View:

• Diagnosed clinically with Fuchs endothelial corneal dystrophy by the study investigator.

• Phakic or pseudophakic with posterior capsule supported, suture-fixated, or sulcus-supported posterior chamber intraocular lens.

• Fuchs dystrophy grades 2-5 on the Krachmer grading scale.

• Presence of central guttae and/or stromal edema being the primary cause of decreased vision.

• The peripheral cornea to the central 6mm is devoid of guttata changes.

• Best corrected visual acuity in the study eye is 20/40 or worse with glare testing at study enrollment.

Locations
United States
Oregon
Devers Eye Institute
RECRUITING
Portland
Contact Information
Primary
Alex J Bauer, B.S.
alex@visiongift.org
503-413-8377
Backup
Michael D Straiko, M.D.
mike.straiko@gmail.com
503-413-8032
Time Frame
Start Date: 2019-03-25
Estimated Completion Date: 2025-02-01
Participants
Target number of participants: 72
Treatments
Experimental: Glanatec
Glanatec eye drops will be administered 6x per day for 2-4 weeks
Placebo_comparator: Placebo Control
Optive artificial tears will be administered 6x per day for 2-4 weeks
Sponsors
Collaborators: Eye Bank Association of America, Lions VisionGift Research
Leads: Michael D. Straiko, MD

This content was sourced from clinicaltrials.gov

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