Corneal Asphericity Adjustment (Q Adjustment) in Myopic and Hyperopic Patients Undergoing Refractive Correction With Excimer Laser

NCT ID: NCT01296867

Last Updated: 2011-02-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

36 participants

Study Classification

OBSERVATIONAL

Study Start Date

2006-03-31

Study Completion Date

2009-05-31

Brief Summary

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To study the postoperative results in myopic and hyperopic eyes treated with two different laser ablation algorithms (STD and F-CAT), both FDA approved.

Detailed Description

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Conditions

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Myopia Hyperopia

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Myopic and hyperopic eyes eligible for LASIK or PRK refractive correction
* Central corneal thickness more than 500 micrometers

Exclusion Criteria

* Topographies of less than 55% of successful total sampled area and eyes exhibiting asphericity variations, in either the horizontal or the vertical axis, greater than 0.2
* Corneal scarring
* Cataract surgery
* Corneal ulceration
* Topographical abnormalities
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Democritus University of Thrace

OTHER

Sponsor Role lead

Responsible Party

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Eye Institute of Thrace / Democritus University

Other Identifiers

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Q-value

Identifier Type: -

Identifier Source: org_study_id

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