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NCT00552019 Clinical Trial

Intraocular Pressure (IOP) Assessed by Dynamic Contour Tonometer (DCT) and Goldman Applanation Tonometry (GAT)

Uveitis Clinical Trial

Official title:
Inflammatory Changes of Corneal Thickness and Influence on Assessment of Intraocular Pressure

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00552019
Other study ID # 2007-405-f-S
Secondary ID
Status Completed
Phase N/A
First received October 31, 2007
Last updated November 17, 2009
Start date October 2007
Est. completion date April 2009

Study information
Verified date November 2009
Source St. Franziskus Hospital
Contact n/a
Is FDA regulated No
Health authority Germany: Federal Ministry of Education and Research
Study type Observational

Clinical Trial Summary

The purpose of this study is to evaluate an assessment of the intraocular pressure with the dynamic contour tonometry and the Goldmann applanation tonometry in patients with active anterior uveitis.

Description:

Keratoprecipitates are often found in anterior uveitis. Also elevation of the IOP can be seen in these patients. Goldmann applanation tonometry is the standard technique to assess the IOP but depends on the corneal thickness. Therefore IOP is measured by Goldmann and dynamic contour tonometry and corneal thickness is quantified by Orbscan at active uveitis and after the keratoprecipitates have disappeared.

Recruitment information / eligibility
Status Completed
Enrollment 30
Est. completion date April 2009
Est. primary completion date April 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- active anterior or panuveitis with keratoprecipitates

Exclusion Criteria:

- corneal endothelial dystrophy

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Germany Department of Ophthalmology at St.-Franziskus Hospital Münster

Sponsors (1)
Lead Sponsor Collaborator
St. Franziskus Hospital

Country where clinical trial is conducted

Germany, 

Outcome
Type Measure Description Time frame Safety issue
Primary IOP by GAT and DCT 3 months after treatment start
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