*The CORIMAP study - A comparison study between a prototype retinal handheld oximeter (CORIMAP camera) and the Oxymap T1*

Completed

• Conditions: retina saturation; retinal oximetry; 10047060

• Registration Number: NL-OMON43401
• Lead Sponsor: eids Universitair Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 30

Inclusion Criteria

Participants with an age between 18 - 35 years

Exclusion Criteria

• Subjects will be excluded in case of pathological findings during the ophthalmologic examination incl. ocular opacity
• Subjects will be excluded if refractive error is lagers than +/- 6.00 dioptres and / or a cylinder of +/- 1.50 dioptres
• Subjects will be excluded in case of any ocular diseases in their history or a familial history of glaucoma.
• Subjects with any systemic disease, which could affect the eye or oxygen levels such as diabetes, respiratory- and cardiovascular disease are excluded.
• Subjects are excluded if they smoke

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The ODR will be determined in three different situations (Sitting, supine and<br /><br>hyperoxic) to make a comparison between the CORIMAP prototype camera and the<br /><br>Oxymap T1. The ODR is inversely linear related to the oxygen saturation.<br /><br>Therefore, the oxygen saturation can be determined in the retinal vessels. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>The secondary study parameter is the measurements of the prototype CORIMAP<br /><br>camera and Oxymap T1 of the diameter of the vessels of the retina in both<br /><br>normoxia and hyperoxia.</p><br>