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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03228784
Other study ID # 5780
Secondary ID
Status Completed
Phase N/A
First received July 14, 2017
Last updated July 22, 2017
Start date June 1, 2013
Est. completion date May 1, 2014

Study information

Verified date July 2017
Source Minia University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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


Recruitment information / eligibility

Status Completed
Enrollment 53
Est. completion date May 1, 2014
Est. primary completion date May 1, 2014
Accepts healthy volunteers
Gender All
Age group 21 Years and older
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
LASIK


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Minia University

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of dry eye Schirmer 1 test in millimeters 6 months
Primary Degree of dryness Tear break up time in seconds 6 months