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 @ 11:24 PM
Ignite Modification Date:
2025-12-24 @ 11:24 PM
NCT ID:
NCT01870856
Eligibility Criteria:
Inclusion Criteria:
* Sign Informed Consent document.
* Severe lid wiper epitheliopathy (upper lid) in either eye.
* Currently wearing spherical daily disposable soft contact lenses or daily wear soft contact lenses in both eyes with at least 3 months of contact lens wearing experience.
* Symptomatic as determined by the SPEED questionnaire.
* Willing to follow visit schedule.
* Habitual contact lens power with the range of -1.00 to -6.00 diopters (D) with best corrected distance visual acuity greater than or equal to 20/25 in each eye.
* Astigmatism less than or equal to 0.75D.
* Possess spectacles which provide visual acuity of at least 20/25 in each eye.
* Willing and able to complete daily diaries.
* Other protocol-defined inclusion criteria may apply.
Exclusion Criteria:
* Eye injury within 12 weeks immediately prior to enrollment.
* Any ocular condition that would contraindicate contact lens wear.
* Any use of systemic or ocular medications that would contraindicate contact lens wear, as determined by the investigator.
* Currently wearing toric or multifocal soft contact lenses.
* Participation in a clinical study (including contact lens or contact lens care product) within the previous 30 days.
* Routinely sleeps in lenses for at least 1 night per week.
* Other protocol-defined exclusion criteria may apply.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT01870856
Study Brief:
Protocol Section:
NCT01870856