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 @ 12:43 AM
Ignite Modification Date:
2025-12-25 @ 12:43 AM
NCT ID:
NCT02517567
Eligibility Criteria:
Inclusion Criteria:
* Sign an informed consent document;
* Adapted, current soft contact lens wearer;
* Symptoms of contact lens discomfort as defined by the Symptomatology (Eligibility) Questionnaire;
* Can be successfully fitted with study lenses;
* Willing to wear lenses for a minimum of 8 hours prior to each study visit;
* Willing to discontinue artificial tears and rewetting drops usage on the days of study visits;
* Other protocol-specified inclusion criteria may apply.
Exclusion Criteria:
* Ocular anterior segment infection, inflammation, abnormality, or active disease that would contraindicate contact lens wear;
* Use of systemic or ocular medications for which contact lens wear could be contraindicated as determined by the investigator;
* Monocular (only 1 eye with functional vision) or fit with only one lens;
* History of herpetic keratitis, ocular surgery, or irregular cornea;
* Known pregnancy and lactation;
* Other protocol-specified exclusion criteria may apply.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT02517567
Study Brief:
Protocol Section:
NCT02517567