N/A
Completed N=186
The Clinical Performance of Two Reusable Silicone Hydrogel Contact Lenses
Refractive Ametropia
Source: ClinicalTrials.gov NCT05766787 ↗
Enrolled (actual)
186
Serious AEs
0.0%
Results posted
Jun 2024
Primary outcomePrimary: Least Squares Mean Distance VA With Study Lenses at Week 1 — -0.11; -0.10 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 Least Squares Mean Distance VA With Study Lenses at Week 1 |
-0.11; -0.10 | — |
Eligibility Criteria
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 (BCVA) 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-specific inclusion criteria may apply.
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 (NCT05766787). 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.