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Cornea Ectasia Excimer Laser Treatment

B

Bambino Gesù Hospital and Research Institute

Status

Completed

Conditions

Corneal Ectasia

Treatments

Procedure: topographic guided trans epithelial excimer laser

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

To evaluate efficacy, safety, objective and subjective quality of vision after treatment of cornea ectasia with transepithelial topographic guided laser simultaneous Central Corneal Remodeling (CCR) and Cross-linking (CXL).

Full description

Background To evaluate efficacy, safety, objective and subjective quality of vision after treatment of cornea ectasia performed with transepithelial topographic guided laser simultaneous Central Corneal Remodeling (CCR) and Cross-linking (CXL).

Methods In this retrospective study 8 eyes of 8 patients (mean age 31.50±14.73 years) affected by cornea ectasia underwent simultaneous CCR and CXL. Preoperative and 6 month postoperative uncorrected distance visual acuity (UDVC) and distance corrected visual acuity (DCVA) were measured using the Efficacy and Safety index. Objective and subjective quality of vision were evaluated preoperatively and 6 months postoperatively using corneal morphological irregularity index (CMI), National Eye Institute Visual Function NEI-VFQ25 and NEI-VFQ39 questionnaires.

Enrollment

8 patients

Sex

All

Ages

19 to 66 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • keratoconus with moderate severity (Amsler-Krumeich stage I-II)

Exclusion criteria

  • concomitant ocular disease
  • concomitant systemic disease
  • corneal opacities

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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