N/A
Completed N=68
Clinical Performance of Two Reusable Silicone Hydrogel Contact Lenses
Source: ClinicalTrials.gov NCT05431478 ↗Enrolled (actual)
68
Serious AEs
0.0%
Results posted
Sep 2023
Primary outcomePrimary: Visual Acuity With Study Lenses at Week 1 Follow-Up — -0.12; -0.11 logMAR
Summary
The purpose of this study is to assess the clinical performance of two reusable silicone hydrogel contact lenses when worn on a daily wear basis.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Visual Acuity With Study Lenses at Week 1 Follow-Up |
-0.12; -0.11 | — |
Eligibility Criteria
Key Inclusion Criteria
- Successful wear of 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 (0.10 logMAR) or better in each eye.
- Willing to stop wearing habitual contact lenses for the duration of study participation.
- Other protocol-specified inclusion criteria may apply.
Key Exclusion Criteria
- Any eye infection, inflammation, abnormality or disease (including systemic) that contraindicates contact lens wear, as determined by the investigator.
- Any use of systemic or ocular medications for which contact lens wear could be contraindicated, as determined by the investigator.
- Habitual wear of AOHP contact lenses.
- Habitual wear of any daily disposable contact lenses.
- Other protocol-specified exclusion criteria may apply.
Data sourced from ClinicalTrials.gov (NCT05431478). 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.