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: 2026-03-26 @ 3:16 PM
Ignite Modification Date: 2026-03-26 @ 3:16 PM
NCT ID: NCT07370168
Eligibility Criteria: Inclusion Criteria: Age between 18 to 40 years * Willing to use the prescribed soft daily disposable contact lenses * Normal ocular health * Rx range from +8.00 to -12.00DS and up to 2.50DC (within range that could be fitted by CV 1 day CLs) * Willing to provide written consent in English * Can attain good vision: Best-corrected visual acuity of 6/12 or better in each eye * Have no history of ocular surgery, injury, recent or current infection within the last 3 months * Have no known allergies to the study products * Willing to attend the scheduled study visits and adhere to instructions * If taking fish oil or tear supplements, should have started at least 3 months prior to starting the study and not planned changes to supplement intake during the study Exclusion Criteria: * RGP, Extended Wear (re-usable), presbyopic, therapeutic/cosmetic, or myopia control contact lens wear * Experienced contact lens wearer with a history of regular lens wear more than 3 months * Unstable refractive error * Binocular vision anomaly not controlled by contact lenses * Patients require Presbyopic correction or age more than 40 years * Age \< 18 years old * Not on a stable medication * Participation in another clinical trial within 2 weeks of participation in this study * History or presence of any ocular disorder or condition in either eye that would likely interfere with the interpretation of the study results or patient safety * Self-reported pregnancy or lactation * Any ocular or systemic condition that may contradict contact lens wear \*\* \*The investigator has the right to exclude any patient's participation in the study if he/she deems it to be in the best interest of the patient. Minor exceptions to the inclusion / exclusion criteria will be submitted to, and considered by, the Pl and approved as required. This includes 'drop-outs' that subsequently return to contact lens wear during the study trial. * OO/CLO (ECP) Clinical Judgement
Healthy Volunteers: True
Sex: ALL
Minimum Age: 18 Years
Maximum Age: 40 Years
Study: NCT07370168
Study Brief:
Protocol Section: NCT07370168