The Effect of Lumify™ on Ocular Redness, Intraocular Pressure, and Eyelid Position in Glaucoma Patients
Starting soon · Phase 4 · Has a placebo group
Conditions studied: Glaucoma, Glaucoma, Open-Angle, Glaucoma; Drugs, Droopy Eyelid, Ptosis, Glaucoma, Primary Open Angle
In brief
Glaucoma represents a group of conditions that cause damage to the optic nerve and can lead to irreversible vision loss. Current treatments are aimed at lowering intraocular pressure while minimizing medication side effects. Lumify™ (Brimonidine Tartrate Ophthalmic Solution 0.025%) is an FDA-approved medication for alleviating eye redness, a common side effect of glaucoma medications. The purpose of this study is to evaluate the effect of Lumify™ on eye redness, intraocular pressure, and eyelid position in patients with glaucoma who are already using the Brimonidine 0.1%, 0.15% or 0.2% eye drops.
Key facts
- Study ID
- NCT04007276
- Run by
- Tulane University
- People needed
- 60
- Starts
- 2026-11-10
- Expected to finish
- 2036-06-01
- Last updated by the study team
- 2025-10-01
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age > 18 years
- Diagnosis of primary open angle glaucoma
- Willing and able to give informed consent
- Current and greater than 6 weeks of brimonidine 0.2%, 0.15% or 0.1% use
You may not qualify if…
- Pregnancy
- Prisoners
- Known allergy or sensitivities to brimonidine
- No surgery within the past 6 months
- No history of lid surgery or botox
- Any other significant ophthalmologic disorder or condition with relevant effect on ocular redness, IOP, or eyelid position as evaluated by principal investigator
- Inability to sit comfortably for 30 minutes
- Prior use of eye whiteners (eg, vasoconstrictors), decongestants, antihistamines, or phenylephrine dilating drops within 1 week of study
Where it is running
- Tulane University Medical Center — New Orleans, Louisiana, United States
Full record on ClinicalTrials.gov
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