Eligibility Module

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 @ 12:04 AM
Ignite Modification Date: 2025-12-25 @ 12:04 AM
NCT ID: NCT02676258
Eligibility Criteria: Inclusion Criteria: * Subject should have normal eyes and use no ocular medications * Subject with -1.00 to -10.00 D myopia, less than 2.00 D astigmatism * VA correctable to Log MAR 0.1 or better. * Willing to comply with all study procedures and be available for the duration of the study. * Provide signed and dated informed consent form. Exclusion Criteria: * Subjects have history of allergies that would contraindicate "normal" contact lens wear. * Subjects have other active ocular or systemic disease such as, but not limited to : anterior uveitis (past or present), glaucoma, Sjögren's syndrome, lupus erythematosus, sclerodermas, keratoconus or type II diabetes. * Subjects have medications that would contraindicate contact lens wear. * Currently pregnant (to the best of the subject's knowledge), is lactating or is planning a pregnancy within the next 3 month. * Current drug or alcohol use or dependence that, in the opinion of the site investigator, would interfere with adherence to study requirements. * Any active participation in another clinical trial within 30 days prior to this study. * The presence of clinically significant (grade 3 or 4) anterior segment abnormalities; inflammations such as iritis; or any infection of the eye, lids, or associated structures. * A known history of corneal hypoesthesia (reduced corneal sensitivity), corneal ulcer, corneal infiltrates or fungal infections. * A history of papillary conjunctivitis that has interfered with contact lens wear.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 20 Years
Study: NCT02676258
Study Brief:
Protocol Section: NCT02676258