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

L

London Vision Clinic

Status

Enrolling

Conditions

Refractive Errors

Treatments

Procedure: PTK-PRK refractive treatment

Study type

Observational

Funder types

Other

Identifiers

NCT06996353
LoVC-011

Details and patient eligibility

About

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.

Full description

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.

The EpiMaster application software is not used in this clinical investigation, consequently, it is a merely observational investigation.

Enrollment

150 estimated patients

Sex

All

Ages

21+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 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

Exclusion criteria

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

Trial contacts and locations

2

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Central trial contact

Timothy Archer, PhD

Data sourced from clinicaltrials.gov

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