Eye redness can be more than just an annoyance—it can impact your comfort, confidence, and daily life. If you frequently experience red, irritated, or bloodshot eyes, you may qualify for a clinical research study evaluating an investigational new eye drop designed to potentially reduce eye redness.
This study will enroll approximately 554 participants across approximately 12 locations. U.S. Eligible participants will be randomized to receive either the investigational eye drop or the LUMIFY eye drop that is currently available on the market. Participants will be closely monitored throughout the study to ensure safety and effectiveness.
Your participation could help advance research for better eye redness treatments while receiving expert care. To see if you qualify, complete the form below, and a team member will reach out to you shortly. Or you can call our study team directly at 1-866-927-0348
You may qualify to participate if you:
You are 18 years or older
You have been experiencing chronic ocular redness
Have used or desire to use eye drops for eye redness in the last 6 months
You have not undergone eye surgery in the last three (3) months or refractive surgery (LASIK) in the last six (6) months
If you qualify for this study, here is what you can expect:
Study Visits: You will attend five study visits over approximately nine (9) weeks.
Study Drug: You will be given the study drug or LUMIFY eye to take home and use along with a dosing diary to complete.
Compensation: You may receive up to $700 – $1,000 for completing all study visits.
During these visits, you will:
In addition, there are other assessments that the study team will discuss with you in detail during your visits.
We are currently conducting this study at these locations. Take a look at our addresses below to find out if the study location is near you.
The study will last approximately two months, with six visits.
Participation in any clinical study is completely voluntary. Your decision to participate will not impact the medical care you currently receive or may receive in the future. If you qualify and choose to join the study, you may withdraw at any time for any reason.
All study-related testing will be provided to you by the sponsor at no charge; however, taking part in this study may lead to added costs to you and/or your insurance company.
Your personal and medical information is completely protected before, during and after the clinical trial process through the HIPAA (Health Insurance Portability and Accountability Act) Privacy Rule. You will also be informed of who has access to your personal information.
Key Inclusion Criteria
Key Exclusion Criteria
Sign up for email alerts when new trials and locations are added for a medical condition.