A Clinical Study to Evaluate the KeraKlear Keratoprosthesis in Patients With Corneal Opacity
Not Applicable
Terminated
- Conditions
- Corneal Blindness
- Interventions
- Device: KeraKlear Non-Penetrating Keratoprosthesis
- First Posted Date
- 2017-04-25
- Last Posted Date
- 2019-12-10
- Lead Sponsor
- KeraMed, Inc.
- Target Recruit Count
- 11
- Registration Number
- NCT03126903
- Locations
- 🇺🇸
Cincinnati Eye Institute, Edgewood, Kentucky, United States
🇺🇸University of California Irvine, Irvine, California, United States
🇺🇸Massachussetts Eye and Ear Infirmary, Boston, Massachusetts, United States
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