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NCT Number: NCT03675412

Caffeine Consumption in Glaucoma Patients and Healthy Subjects

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.

Recruiting

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Key information

Age range

18 year–90 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Wills Eye Glaucoma Service

Philadelphia, Pennsylvania, 19107, United States

Location status: Recruiting

Location contact

Anand Montravadi, MD

SUB_INVESTIGATOR

Jay L Katz, MD

SUB_INVESTIGATOR

Jeanne Molineaux, COA

CONTACT

[email protected]

215-825-4713

Jonathan S Myers, MD

SUB_INVESTIGATOR

Marlene R Moster, MD

SUB_INVESTIGATOR

Michael J Pro, MD

SUB_INVESTIGATOR

Scott Fudemberg, MD

SUB_INVESTIGATOR

About this study

Ingestion of caffeine in glaucoma patients and healthy subjects may decrease peripapillary and macular blood flow in the back of the eye.

The primary objective of this study is to assess the acute changes in peripapillary and macular blood flow before and after an intake of oral caffeine (200 milligram tablet) in glaucoma patients and healthy subjects by using optical coherence tomography angiography (OCTA) scans. This novel imaging tool creates three-dimensional angiograms to assesses signal changes caused by flowing blood cells in a non-invasive angiogram scan. Blood flow is shown as vessel density measured in percentage.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • age 18 to 90 years
  • diagnosis of primary open angle glaucoma (Mild, Moderate and Advanced)
  • healthy subjects with no eye disease

Exclusion criteria

  • Diseases, ophthalmic or systemic, that are likely to affect OCTA results
  • greater than moderate cataract
  • nystagmus
  • inability to look at target
  • macular degeneration other than mild drusen or pigmentary changes
  • diabetic retinopathy
  • neovascular glaucoma or non-glaucoma optic neuropathies
  • current macular edema, prior laser to retina, inflammatory retinopathy or choroidopathy
  • keratoconus, corneal ectasia, central corneal scarring
  • rheumatologic diseases or Raynaud's phenomena
  • pregnant and lactating women
  • mental illness or alcohol addiction
  • pre-existing bladder symptoms, cardiac disease or sleep disorder
  • refractive spherical diopter greater than 5 or cylinder greater than 3
  • possible tolerance to caffeine (drinking more than 1 cup coffee per day).

Treatment and study plan

Caffeine tablet

Dietary Supplement

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

Primary outcomes

  1. Blood flow change in back of eye before and after caffeine

    Time frame: Baseline, Hour 1, Hour 2

    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.

Study contacts

Contact information is provided by the study sponsor or research team.

Jeanne Molineaux, COA

CONTACT

[email protected]

215-825-4713

M. Reza Razeghinejad, MD

CONTACT

[email protected]

215-928-7023

Sponsors and collaborators

Lead sponsor

Wills Eye

Other

Registry information

Official study title

Acute Changes in Optic Nerve Head (ONH) and Macular Blood Flow After Caffeine Consumption in Glaucoma Patients and Healthy Subjects: A Quantitative Optic Coherence Tomography Angiography (OCTA) Study

Important dates

Study start
2018
Primary completion
2026
Study completion
2026
First posted
Sep 18, 2018
Registry last updated
Nov 14, 2025

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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