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OpenTrials
Completed

NCT Number: NCT00552019

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

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Department of Ophthalmology at St.-Franziskus Hospital

Münster, 48145, Germany

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • active anterior or panuveitis with keratoprecipitates

Exclusion criteria

  • corneal endothelial dystrophy

Treatment and study plan

Primary outcomes

  1. IOP by GAT and DCT

    Time frame: 3 months after treatment start

Sponsors and collaborators

Lead sponsor

St. Franziskus Hospital

Other

Registry information

Official study title

Inflammatory Changes of Corneal Thickness and Influence on Assessment of Intraocular Pressure

Important dates

Study start
2007
Primary completion
2009
Study completion
2009
First posted
Nov 1, 2007
Registry last updated
Nov 18, 2009

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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