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Dry Eye Evaluation After Transepithelial PRK

Not Applicable
Completed
Conditions
Dry Eye
Registration Number
NCT02210793
Lead Sponsor
AL-Nour Eye Hospital
Brief Summary

The aim of the study is to evaluate the severity of dry eye syndrome following excimer laser vision correction using no-touch all-laser photorefractive keratectomy in comparison to conventional lasik

Detailed Description

Prospective interventional clinical study 2 groups: Group A : 20 eyes of 10 patients undergoing transepithelial PRK Group B: 20 eyes of 10 patients undergoing LASIK using mechanical microkeratome Tear Break Up Time and Schirmer 2 tests are used to evaluate severity of dry eye before surgery and 1 , 3 and 6 months postoperative Follow up period : 6 months

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
40
Inclusion Criteria

Not provided

Exclusion Criteria
  • Pregnancy and lactation
  • Keratoconus
  • Previous refractive surgery
  • Previous herpetic keratitis

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
qualitative assessment of dry eye syndrome6 months

Tear Break Up time is used as a qualitative measure of dry eye after surgery

quantitative of dry eye after surgery6 months

Schirmer test is used as a quantitative measure of dry eye after surgery

Secondary Outcome Measures
NameTimeMethod
haze6 months

haze is a known possible complication of surface ablation Its severity can be graded according to a slit lamp scoring system

Trial Locations

Locations (1)

Al Nour Eye Hospital

🇪🇬

Giza, Egypt

Al Nour Eye Hospital
🇪🇬Giza, Egypt

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