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OpenTrials
Completed

NCT Number: NCT02189447

Photorefractive Keratectomy and Corneal Cross-linking in Keratoconus

Evaluation of the safety and efficacy of surface ablation followed by Collagen Cross-linking in patients with keratoconus

Completed

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • contact lens intolerance
  • corneal thickness > 450 micrometers
  • Keratometry < 56 diopters
  • Astigmatism < 6 diopters

Exclusion criteria

  • corneal thickness < 450 micrometers
  • Keratometry > 56 diopters
  • Astigmatism > 6 diopters

Treatment and study plan

Simultaneous Photorefractive Keratectomy and Collagen Cross-linking in patients with keratoconus

Procedure

Photorefractive Keratectomy followed by Collagen Cross-linking in patients with keratoconus in the same surgical setting

Primary outcomes

  1. The change of visual acuity following Photorefractive Keratectomy and Corneal Collagen Cross-linking in patients with Keratoconus

    Time frame: 6 months

    The change of visual acuity from baseline in patients suffering from keratoconus following treatment with Photorefractive Keratectomy and Corneal Collagen Cross-linking.

Sponsors and collaborators

Lead sponsor

The Eye Center and The Eye Foundation for Research in Ophthalmology

Other

Registry information

Important dates

Study start
2011
Primary completion
2013
Study completion
2013
First posted
Jul 14, 2014
Registry last updated
Jul 14, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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