Evaluation of Comfort in Subjects With Moderate Dry Eye Disease

  • STATUS
    Recruiting
  • days left to enroll
    21
  • participants needed
    30
  • sponsor
    Alcon Research
Updated on 13 August 2021

Summary

The purpose of this study is to evaluate the comfort of an ocular lubricant in dry eye subjects. This study will be conducted in Canada and Australia.

Details
Condition Dry eye syndrome, Keratoconjunctivitis Sicca, Dry Eyes, eye dryness, dry eye
Treatment FID123238, Systane Hydration
Clinical Study IdentifierNCT04830956
SponsorAlcon Research
Last Modified on13 August 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Able to understand and sign an information consent letter
Willing and able to follow instructions and maintain the appointment schedule
Has dry eye symptoms

Exclusion Criteria

Has suffered any ocular injury to either eye in the past 12 weeks
Is pregnant or lactating at the time of enrollment
Other protocol-specified inclusion/exclusion criteria may apply
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How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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