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German Corneal Cross Linking Register

S

Suphi Taneri

Status

Active, not recruiting

Conditions

Keratoconus

Treatments

Procedure: CCL (Corneal Cross Linking)

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

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

Enrollment

7,500 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients diagnosed with keratokonus and treated with corneal cross Linking in Germany

Exclusion criteria

  • Non-ectatic conditions

Trial design

7,500 participants in 1 patient group

1
Description:
Cross linked eyes
Treatment:
Procedure: CCL (Corneal Cross Linking)

Trial contacts and locations

2

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Central trial contact

Suphi Taneri, MD; Anika Förster, MSc

Data sourced from clinicaltrials.gov

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