Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 1:00 PM
Ignite Modification Date:
2025-12-24 @ 1:00 PM
NCT ID:
NCT00532961
Eligibility Criteria:
Inclusion Criteria:
* in good general health based on investigator judgment
* able and willing to follow instructions, provide informed consent, make the required study visits, and use an electronic patient diary during the study
* possessing a best corrected visual acuity of at least 20/40 in each eye
* for females, using reliable contraception and a negative urine pregnancy test prior to study entry
Exclusion Criteria:
* contact lenses worn within 30 days prior to enrollment or during study period
* known hypersensitivity to study medication or any component
* presence of significant ocular or systemic disease that might interfere with the interpretation of the results
* a need for administration of chronic topical ocular or systemic medications of any kind during the study.
* participation in an opthalmic drug or device research study within 30 days prior to entry
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT00532961
Study Brief:
Protocol Section:
NCT00532961