Clinical Trials Directory

Trials / Completed

CompletedNCT01023997

Central Corneal Thickness in Glaucoma

Central Corneal Thickness in Patients With Exfoliation Syndrome, Exfoliative Glaucoma, Exfoliative Glaucoma, Primary Open-angle Glaucoma and Ocular Hypertension

Status
Completed
Phase
Study type
Observational
Enrollment
700 (actual)
Sponsor
Aristotle University Of Thessaloniki · Academic / Other
Sex
All
Age
25 Years – 89 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to compare the central corneal thickness measurement in patients with exfoliation syndrome, exfoliative glaucoma, primary open-angle glaucoma, ocular hypertension and normal controls and to evaluate the value of corneal thickness in the diagnosis and management of glaucoma.

Detailed description

To compare the central corneal thickness measurement in patients with exfoliation, primary open-angle glaucoma, ocular hypertension and normal controls and to evaluate the value of corneal thickness in the diagnosis and management of glaucoma. Prospective study in progress. Randomly selected patients undergo a comprehensive ophthalmic exam which includes 2 separate pachymetry measurements in 2 different examinations at the same time of the day (10:00 am) with 3 different pachymeters. The values obtained are correlated with a number of other glaucoma parameters. A thinner cornea may represent a specific attribute and an additional risk factor for patients with exfoliation. Evaluation of corneal thickness is an important exam in the management of patients with exfoliation.

Conditions

Timeline

Start date
2008-01-01
Primary completion
2013-01-01
Completion
2013-01-01
First posted
2009-12-02
Last updated
2014-05-12

Locations

1 site across 1 country: Greece

Source: ClinicalTrials.gov record NCT01023997. Inclusion in this directory is not an endorsement.