The primary goal of this study is to determine if excimer laser smoothing of the cornea
before Descemet's stripping automated endothelial keratoplasty (DSAEK)improves postoperative
Best Spectacle Corrected Visual Acuity (BSCVA).
Procedure: DSAEK with graft shaping and smoothing
Procedure: Standard DSAEK
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Locations near you
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Full eligibility criteria for NCT01586234
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Adults with visual complaint and objective evidence of decreased vision due to corneal edema related to Fuchs' corneal endothelial dystrophy
Inability to give informed consent
Inability to maintain stable fixation for OCT imaging
Inability to commit to required visits to complete the study
Eyes with concurrent cataract, retinal diseases, glaucoma, or other eye conditions that may limit the visual outcome after surgery
All locations for NCT01586234
United States (1)
Devers Eye Insitute
Portland, Oregon, United States, 97210
View full eligibility
Tris trial is registered with FDA with number: NCT01586234. The sponsor of the trial is Oregon Health and Science University and it is looking for 6 volunteers for the current phase.
Official trial title: Randomized Clinical Trial of OCT-guided DSAEK Graft Shaping and Smoothing
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