Clinical Data Collection of Myopic Patients After PTK-PRK With CZM MEL 90 Excimer Laser

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorLondon Vision Clinic

About this trial

The objective of the clinical investigation presented to is to verify predictions of post-operative PTK-PRK refractive outcome made by the EpiMaster application software by comparing these to post-operative clinical data after routine PTK-PRK treatments.

Eligibility criteria

Qualifiers

Inclusion criteria are according to the user manual of CZM MEL 90 Excimer Laser for treatment of refractive errors

Patient present with myopic or myopic and astigmatic error

Patient will be able to understand the patient information and willing to sign an informed consent

Patient will be willing to comply with all follow-up visits and the respective examinations

Disqualifiers

Exclusion criteria are according to the user manual of CZM MEL 90 Excimer Laser for treatment of refractive errors

Trial design

Treatments tested in this trial

  • PTK-PRK refractive treatment

Treatment groups

No treatment groups listed

Sponsors and collaborators

London Vision Clinic

Lead sponsor

Optana GmbH

Collaborator