Can a simple eye treatment stop the need for a corneal transplant?
NCT ID NCT00560651
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This registry collects long-term data from hundreds of people in Germany who have undergone corneal cross linking for keratoconus, a condition where the cornea thins and bulges, causing vision loss. The procedure uses riboflavin (vitamin B2) eye drops and UV light to stiffen the cornea and stop the disease from getting worse. The goal is to see whether this treatment can prevent the need for a corneal transplant over time.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Corneal cross linking (riboflavin plus UV light)
- What this could lead to
- If successful, this registry could confirm that corneal cross linking stops keratoconus from worsening and reduces the need for corneal transplants.
- What could go wrong
- This is an observational registry, not a controlled trial, so it cannot prove cause and effect. Rare complications or limited long-term data may affect conclusions.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
356 people
The number who actually took part.
- Started
-
Nov 2007
- Expected to finish
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Nov 2027
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients treated with Corneal Cross Linking in Germany
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients diagnosed with keratokonus and treated with corneal cross Linking in Germany Exclusion Criteria: * Non-ectatic conditions
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Augenklinik am St. Franziskus Hospital
Münster, 48145, Germany
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University of Saar
Homburg, 66421, Germany
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Shorter eye treatment put to the test against standard crosslinking
- Shorter UV treatment for keratoconus put to the test
- Insulin eye drops put to the test for faster corneal healing
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