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OpenTrials
Completed

NCT Number: NCT03228784

The Effect of Ablation Depth on Dry Eye After LASIK Treatment of Myopia

The study tried to find the relation between ablation depth and degree of dryness after LASIK treatment of myopic patients

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Key information

Age range

21 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

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

Inclusion criteria

  • Patients with age ≥ 21 years
  • Normal Pentacam maps
  • Myopia with spherical equation less than 12 D
  • Corneal thickness ≥ 500 Microns
  • Calculated residual stromal bed ≥ 280 microns
  • No signs or symptoms of dry eye.

Exclusion criteria

  • Keratoconus and forme fruste keratoconus
  • Auto-immune diseases
  • History of dry eye or previous use of tear substitutes
  • Previous ocular surgery
  • Pregnant or lactating women.

Treatment and study plan

LASIK

Procedure

Other names: Corneal Flap creation with mechanical microkeratome and stromal ablation with Excimerr laser.

Primary outcomes

  1. Incidence of dry eye

    Time frame: 6 months

    Schirmer 1 test in millimeters

  2. Degree of dryness

    Time frame: 6 months

    Tear break up time in seconds

Sponsors and collaborators

Lead sponsor

Minia University

Other

Registry information

Important dates

Study start
2013
Primary completion
2014
Study completion
2014
First posted
Jul 25, 2017
Registry last updated
Jul 25, 2017

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.