N/A
Completed N=162
Clinical Assessment of Two Reusable Silicone Hydrogel Contact Lenses
Source: ClinicalTrials.gov NCT05050578 ↗Enrolled (actual)
162
Serious AEs
0.0%
Results posted
Mar 2023
Primary outcomePrimary: Least Squares Mean Distance Visual Acuity With Study Lenses at Day 30 — -0.07; -0.07 logMAR
Summary
The purpose of this study is to compare the clinical performance of LID018869 soft contact with ACUVUE® OASYS with HYDRACLEAR® PLUS (AOHP) soft contact lenses over 30 days of daily wear.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Least Squares Mean Distance Visual Acuity With Study Lenses at Day 30 |
-0.07; -0.07 | — |
Eligibility Criteria
Key Inclusion Criteria
- Current wearer of a commercial spherical weekly/monthly soft contact lenses 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 in each eye.
- Best corrected distance visual acuity better than or equal to 20/25 Snellen in each eye.
- Other protocol-defined inclusion criteria may apply.
Key Exclusion Criteria
- Monovision or multifocal lens wearer.
- Habitual senofilcon contact lens wearer (for example, Acuvue Oasys, Acuvue Vita) or commercially available lehfilcon A contact lens wearer (TOTAL30).
- Routinely sleeps in habitual contact lenses.
- Other protocol-defined exclusion criteria may apply.
Data sourced from ClinicalTrials.gov (NCT05050578). 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.