Adults needed for an Ocular Redness treatment study.
You may qualify!

About the Study

Ocular (eye) redness is an extremely common condition that can be caused by minor irritations. Researchers are working on a new therapy to relieve eye redness.

A new topical (eye drop) medication to treat the signs and symptoms of ocular redness is being developed by Alcon. This investigational eye drop was previously studied and showed potential for both fast and long-lasting redness relief. It may even provide beyond 12 hours of redness relief. Researchers hope this new therapy can prove to be both safe and effective, allowing people with ocular redness to experience longer lasting relief without the inconvenience of frequently using eye drops.

This study is studying the preservative free version of the investigational medication. At the second visit, participants will be given one drop into each eye by the investigator/site staff. There are a total of three visits over approximately nine days and participants will come into a clinic and undergo several non-invasive eye exams and questionnaires. Participants who enroll may also receive compensation of up to $XXX for their time and effort.

To see if you qualify, complete the form below. Our team will reach out to ask a few questions and provide more details.

Who Can Participate

You may qualify to participate if you:

Are 18 years or older 

Have used or wanted to use eye drops for ocular redness relief in the last six months. 

Have NOT had eye surgery in the past six months

Have no major ocular conditions other than ocular redness

 

What Can You Expect

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If you qualify for this study, here is what you can expect: 

  • Study Visits: You will be asked to attend three in-clinic visits over approximately nine days.
  • Study Drug: The study drug is in the form of an eye drop and will be given to you in office by the site staff. There will be no at home administration. This study also includes a placebo. Therefore, there is a chance (50/50) that you may be assigned to the placebo group during the study. The study doctor and staff will not know which study drug you are assigned, unless a medical emergency arises.
  • Compensation: You may receive up to $XXX for your time and effort.

During this visit you will go through a series of assessments, including:

  • Medical History Review: You will be asked about your overall health, past medical conditions, medications, and previous eye treatments.
  • Eye Exams: Various eye examinations to assess your eye
  • Questionnaires: You will complete simple surveys about your experiences and the eye drop itself.

Study Locations

 

This study is currently being conducting nationwide across the United States. Review our current locations below to find a study site nearest you.

  • Advancing Vision Research | 515 Stonecrest Parkway Suite 210, Smyrna, TN 37167
  • Aesthetic Eyecare Institute & Eye Research Foundation | 520 Superior Avenue, Suite 235, Newport Beach, CA 92663
  • Butchertown Clinical Trials | 205 N. Spring St., Louisville, KY 40206
  • Global Research Management | 1510 S Central Ave #300, Glendale, CA, 91204 
  • Kanarr Eye Care | 101 N. Broadway, Pittsburg, Kansas 66762
  • NC Eye Association | 1429 Kelly Rd, Apex, NC 27502
  • NVision | 23441 Madison St. Unit #120, Torrance, CA 90505
  • Scott & Christie | 105 Brandt Dr # 201, Cranberry Twp, PA 16066

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Frequently Asked Questions

The study will last approximately nine (9) days and includes three (3) clinic visits.

No. You must be a reasonably healthy person with no active ocular infections or other major eye conditions like dry eye disease or eye allergies. You will be assessed and scored based on your eye redness. If you commonly experience ocular redness, you may be eligible to participate in this study. 

Taking part in any clinical study is entirely voluntary. Your decision whether to participate will not affect 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 and for any reason.

All study-related testing will be provided to you by the sponsor at no charge; Any tests and procedures that are routine care for your eye condition (not part of this research study) may be billed to your insurance. 

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.

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