Louisville, KYNCT07531043Now EnrollingIRB Ready

Ocular Hyperemia Clinical Trial in Louisville, KY

Access cutting-edge ocular hyperemia treatment through this phase 3 clinical trial at a research site in Louisville. Study-provided care at no cost to qualified participants.

Sponsored by Alcon Research

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Expert Care in Louisville

Access ocular hyperemia specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related ocular hyperemia treatment provided free

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Check if you qualify for this ocular hyperemia clinical trial in Louisville, KY

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Louisville

    Convenient for KY residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Louisville site if eligible
  4. 4Begin participation

About This Ocular Hyperemia Study in Louisville

The purpose of this study is to evaluate the efficacy and safety of an investigational ophthalmic solution in adults with ocular redness due to minor eye irritations.

Sponsor: Alcon Research

Who Can Participate

Inclusion Criteria

Capable of giving signed informed consent and comply with the requirements listed in the Informed Consent Form.
Willing and able to follow all instructions and attend all study visits.
History of redness relief eyedrop use within the last 6 months, or an interest in using over-the-counter redness relief drops, or would benefit from the use of redness relief drops in the investigator's opinion.
Baseline investigator-assessed ocular redness score of 0.5 or higher in at least one eye at Visit 1 when applicable and a score of greater than 1.0 in both eyes on a 5-point scale prior to randomization on Day 1 (Visit 2).
Other protocol-defined inclusion criteria may apply. Key

Exclusion Criteria

Known contraindications or sensitivity to the use of any of the investigational product(s) or their components, or any other medication required by the protocol.
Ocular surgical intervention within 6 months prior to Visit 1 or during the study.
Any ocular condition that, in the opinion of the investigator, may compromise the subject's safety or study specific parameters.
Use of any of the prohibited medications or devices as specified in the study protocol.
Out-of-range vital signs (blood pressure and/or pulse rate) as defined in the study protocol.
Abnormal intraocular pressure.
Other protocol-defined exclusion criteria may apply.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Louisville?

Yes, this clinical trial (NCT07531043) has an active research site in Louisville, KY that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Ocular Hyperemia Treatment Options in Louisville, KY

If you're searching for ocular hyperemia treatment options in Louisville, KY, this clinical trial (NCT07531043) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Louisville research site is actively enrolling participants for this phase 3 clinical trial. You'll receive care from experienced ocular hyperemia specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all ocular hyperemia clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Louisville, KY