Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Indiana University
With
Alcon Research
Age
18–any
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Adults\>=18 years of age
Corrected visual acuity of 20/100 or better in both eyes
Ocular Surface Disease Index \[OSDI\] scores between 23 and 50 units \[inclusive\]
Tear break up time score of \<=5 seconds in both eyes
Schirmer I test (without anesthesia) \>=5 mm in both eyes
You may not be if
Discontinue contact lens wear starting 7 days prior and throughout the study
Artificial tears and warm compresses should not be used for at least one week prior to enrollment and throughout the study
Systemic health conditions that are known to alter tear film physiology(e.g., primary and secondary Sjogren's syndrome)
History of ocular surgery within the past 12 months
History of severe ocular trauma, active ocular infection or inflammation, have ever used Accutane or are currently using ocular medications.
Women who are pregnant or breast feeding(self report)
Subjects with a condition or in a situation, which in the investigator's opinion, may put the subject at significant rist, may confound the study results, or may significantly interfere with their participation in the study
Subjects will not be allowed to use any other topical eye drops or other dry eye treatments beyond their assignment during the study
Participants in clinical trial or study using a device, topical, or oral therapeutic in the past 3 months of enrollment
