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Clinical Trials/KCT0004602
KCT0004602
Recruiting
未知

To investigate the effect of dry eye syndrome after Laser Asisted Sub-Epithelial Keratomileusis(LASEK) on ocular and peripheral nerve stimulation: Single blind, Sham controlled, prospective study.

u Eyne0 sites24 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
u Eyne
Enrollment
24
Status
Recruiting
Last Updated
5 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
5 years ago
Study Type
Interventional Study
Sex
All

Investigators

Sponsor
u Eyne

Eligibility Criteria

Inclusion Criteria

  • 1\. 19(Years old) \~ 60(Years old) both of Male, Female
  • 2\. Patients scheduled for LASEK(Laser Epithelial Keratectomy)
  • 3\. The person who met with Grade II Korean Corneal Disease study group's Dry eye disease diagnosis guideline
  • 4\. OSDI \=13
  • 5\. Those who do not have a pregnancy plan during the clinical trial period and have agreed to a contraceptive plan for women of childbearing potential.
  • 6\. A voluntary written consent to participate in this clinical trial

Exclusion Criteria

  • 1\. Have an uncontrolled systemic chronic disease (ex. Diabetes)
  • 2\. The person who has allergic reaction to medicines such as Fluorescein Solution or eye drops.
  • 3\. The person who has a history of ophthalmic surgery that has been known to affect the tear layer within the last 6 months (eg. cataracts, pterygium surgery, etc.)
  • 4\. Systemic drug users (tetracycline derivatives, antihistamine, isotretinoin)
  • 5\. Eyelid Disease or Structural Abnormalities
  • 6\. If there is an acute infection or inflammation of the eye that is not related to Meibomian gland dysfunction
  • 7\. What is wrong with the eyelids or eyelashes
  • 8\. There is an ocular condition or ophthalmic disease that the operation is deemed inappropriate (eg, retinal detachment, glaucoma, etc.).
  • 9\. Pregnant or lactating women
  • 10\. The person who cannot understand or cannot read the consent form of this study (ex. Illiterate or foreign)

Outcomes

Primary Outcomes

Not specified

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