Caffeine Consumption in Glaucoma Patients and Healthy Subjects

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-90
SponsorWills Eye

About this trial

Caffeine is the most widely consumed drinking nutrient in the world. Caffeine effects various organs and the vascular system. It decreases ocular blood flow due to vasoconstriction.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

age 18 to 90 years

diagnosis of primary open angle glaucoma (Mild, Moderate and Advanced)

healthy subjects with no eye disease

Disqualifiers

Diseases, ophthalmic or systemic, that are likely to affect OCTA results

greater than moderate cataract

nystagmus

inability to look at target

Trial design

Design model

Parallel

Treatments tested in this trial

  • Caffeine tablet

    Dietary supplement

    Each eligible participant will receive one 200 mg caffeine tablet to ingest after completing all baseline study tasks.

Treatment groups

80 Participants
are divided into 2 treatment groups
Group A: Glaucoma PatientsActive comparator 1 intervention
Group B: Healthy controlsActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Blood flow change in back of eye before and after caffeine

Optical Coherence Tomography Angiography (OCTA) will be obtained using the Avanti AngioVue High Definition (HD) OCTA by Optovue. Images will include standard 4.5mm HD disc scan, 6mm HD retina scan, regular optic nerve head (ONH) structural scan, 3D-disc baseline scan and a regular ganglion cell complex analysis (GCCA) structural scan. This will measure blood flow changes in the back of the eye by imaging vessel density in percentage before then 1 and 2 hours after caffeine.

Time frame
Baseline, Hour 1, Hour 2

Secondary outcomes

Other outcomes

Sponsors and contacts

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