N/A
Completed N=96
Clinical Assessment of a Daily Disposable Soft Silicone Hydrogel Contact Lens
Refractive Errors
Source: ClinicalTrials.gov NCT06044948 ↗
Enrolled (actual)
96
Serious AEs
0.0%
Results posted
Nov 2024
Primary outcomePrimary: Distance VA With Study Lenses at Week 1 — 95; 92; 5 eyes
Summary
The purpose of this study is to assess the clinical performance of DAILIES TOTAL1® spherical soft contact lenses over approximately 1 week of daily wear.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Distance VA With Study Lenses at Week 1 |
95; 92; 5 | — |
Eligibility Criteria
Key Inclusion Criteria
- Current wearer of commercial spherical soft contact lenses in both eyes with at least 3 months of wearing experience, with a minimum wearing time of 5 days per week and 10 hours per day;
- Manifest cylinder less than or equal to 0.75 diopter (D) in each eye;
- Best corrected distance visual acuity better than or equal to 20/25 (Snellen) in each eye.
Key Exclusion Criteria
- Current or prior habitual DAILIES TOTAL1 soft contact lens wear in the past 3 months prior to consent;
- Monovision contact lens wear;
- Wearing habitual contact lenses in an extended wear modality (routinely sleeping in lenses for at least 1 night per week) over the last 3 months prior to enrollment.
Data sourced from ClinicalTrials.gov (NCT06044948). 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.