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:
2025-12-25 @ 5:03 AM
Ignite Modification Date:
2025-12-25 @ 5:03 AM
NCT ID:
NCT01120418
Eligibility Criteria:
Inclusion Criteria:
* Must have pin-holed Snellen visual acuity equal to or better than 20/40, in both eyes
* Must be in good health (no current or past relevant medical/ocular history) based on the judgment of the Investigator
* Must be willing to discontinue contact lens wear for the duration of the study
Exclusion Criteria:
* Known hypersensitivity to fourth generation fluoroquinolone (SS734) or to any of the ingredients in the study medication Investigator determines could interfere with the study
* History of extended or continuous wear contact lens use other than silicone hydrogels
* History of intraocular surgery
* Any topical ophthalmic medication, including tear substitutes, that cannot be discontinued during the study
* Participation in an ophthalmic drug or device research study within the 30 days prior to entry in this study
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT01120418
Study Brief:
Protocol Section:
NCT01120418