N/A Completed N=66 Randomized Double-blind Treatment

Clinical Comparison of 4 Daily Disposable Soft Contact Lenses

Refractive Error

Source: ClinicalTrials.gov NCT03349632 ↗

Enrolled (actual)

Serious AEs

0.0%

Results posted

Feb 2019

Primary outcomePrimary: Overall Quality of Vision — 8.5; 9.2; 8.8; 9.4 units on a scale

Summary

The purpose of this study is to obtain on-eye performance data to inform contact lens product development and to further evaluate product performance in the intended population.

Outcome Measures

Outcome	Result	p-value
PRIMARY Overall Quality of Vision	8.5; 9.2; 8.8; 9.4; 9.2; 8.8	—

Eligibility Criteria

Inclusion Criteria

Able to understand and must sign an approved Informed Consent Form
Successfully wears daily disposable spherical soft contact lenses in both eyes for a minimum of 5 days per week and 8 hours per day during the past 3 months
Best Corrected Visual Acuity of 20/25 Snellen or better in each eye
Willing to stop wearing habitual contact lenses for the duration of study participation
Other protocol-defined inclusion criteria may apply

Exclusion Criteria

Any eye condition, surgery, disease, or use of medication that contraindicates contact lens wear, as determined by the Investigator.
Routinely sleeps in habitual contact lenses
Currently wears Oasys 1-Day, MyDay, or Moist contact lenses
Other protocol-defined exclusion criteria may apply

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03349632). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.