ight on glaucoma: study to measure contrast sensitivity, visual field, and adaptation time at high light conditions.

Completed

• Conditions: glaucoma; POAG; 10018307

• Registration Number: NL-OMON43212
• Lead Sponsor: niversitair Medisch Centrum Groningen

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 23 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 60

Inclusion Criteria

Glaucoma patients aged 40-70 years who visit the ophthalmology outpatient department of the UMCG, provide written informed consent form and meet in- and exclusion criteria. ;Healthy subjects will consist of people who have signed in, without ophthalmic abnormalities and provide written informed consent.

Exclusion Criteria

Glaucoma patients:
* Visual acuity below 1.0 (below 50 years of age) or below 0.8 (above 50 years).
* Visual field defects not caused by glaucoma. ;Healthy subjects:
* Subjects with an eye disease.
* Subjects with a first grade relative with glaucoma, or with high eye pressure in the past.
* Visual acuity below 1.0 (below 50 years of age) or below 0.8 (above 50 years).
* Visual field defects which are not understood.

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Measurement of contrast sensitivity, visual field and adaptation time at high<br /><br>light conditions. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>N/A</p><br>