The Effect of Lumify™ on Ocular Redness, Intraocular Pressure, and Eyelid Position in Glaucoma Patients

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorTulane University

About this trial

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.

Eligibility criteria

Qualifiers

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

Disqualifiers

Pregnancy

Prisoners

Known allergy or sensitivities to brimonidine

No surgery within the past 6 months

Trial design

Treatments tested in this trial

  • brimonidine tartrate ophthalmic solution 0.025%
  • sterile balanced saline solution

Treatment groups

60 Participants
are divided into 2 treatment groups

Sponsors and collaborators