N/A
Completed N=104
Clinical Performance of Two Frequent Replacement Silicone Hydrogel Multifocal Contact Lenses
Source: ClinicalTrials.gov NCT06469242 ↗Enrolled (actual)
104
Serious AEs
0.0%
Results posted
Oct 2025
Primary outcomePrimary: Mean Binocular Visual Acuity at Distance (4 Meters) at Week 1 — -0.08; -0.08 logMAR
Summary
The purpose of this study is to evaluate the on-eye multifocal clinical performance of investigational LID233309 contact lenses and Oasys multifocal (MF) contact lenses in a daily wear dispensing trial.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Mean Binocular Visual Acuity at Distance (4 Meters) at Week 1 |
-0.08; -0.08 | — |
Eligibility Criteria
Key Inclusion Criteria
- Current wearer of biweekly/monthly replacement multifocal soft contact lenses in both eyes for a minimum of 5 days per week and 10 hours per day during the past 6 months.
- Manifest cylinder equal to or less than 0.75 diopter (D) in each eye.
- Able to wear contact lenses within the available power range with a near ADD of +0.75 D to +2.50 D in each eye.
- Other protocol-defined inclusion criteria may apply.
Key Exclusion Criteria
- Currently pregnant or lactating.
- History of amblyopia, strabismus, or binocular vision abnormalities.
- Habitual Oasys MF contact lens wearers or daily disposable contact lens wearers.
- Monovision contact lens wearers and wearers of contact lens in one eye only.
- Other protocol-defined exclusion criteria may apply.
Data sourced from ClinicalTrials.gov (NCT06469242). 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.