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Clinical Trial Summary

Corneal Cross Linking is new treatment modality for patients with keratoconus. A keratoconus is characterized by progressive bulging and thinning of the eye's cornea. Keratoconus is a potentially severely sight impairing condition that may necessitate corneal transplantation in the progressive state. Corneal Cross Linking is designed to - increase the cornea's mechanical stability - to stop progression of bulging and thinning of the cornea - to prevent the need for corneal transplantation Corneal Cross Linking is performed by 1. Applying Riboflavin (Vitamin B2) eye drops every 2 minutes for 30 minutes to the cornea 2. Illuminating the cornea with UV-light This register of Corneal Cross Linking procedures performed in Germany serves to - gather long-term results - detect rare complications and side-effects - evaluate the efficacy in a large number of patients


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00560651
Study type Observational
Source St. Franziskus Hospital
Contact Suphi Taneri, MD
Phone 49-251-987-7890
Email taneri@refraktives-zentrum.de
Status Recruiting
Phase
Start date November 2007
Completion date November 2027

See also
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