18 and older, any sex, with Refractive Errors. Patients with the condition only — healthy volunteers not accepted.
Results — posted to ClinicalTrials.gov
Per-arm endpoint measurements with 95% confidence intervals where reported. Source: trial results section.
Visual Acuity With Study Lenses at Week 1 Follow-UpPrimary· Week 1, each wear period. A wear period was approximately 14 days.
Visual acuity (VA) was assessed with study lenses in place using logarithmic of the Minimum Angle of Resolution (logMAR) charts. A logMAR acuity of 0.0 corresponds to 20/20 Snellen acuity (normal visual acuity), with a negative value denoting better than 20/20 visual acuity. Each eye was assessed individually. No hypothesis testing was pre-specified for this endpoint.
Group
Value
95% CI
LID022821
-0.12
± 0.07
AOHP
-0.11
± 0.08
Sponsor's own description
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.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
NCT05766787 — The Clinical Performance of Two Reusable Silicone Hydrogel Contact Lenses
· NA
· completed
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Trials by the same sponsor.
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Sponsor: as reported to ClinicalTrials.gov by Alcon Research
Last refreshed: 21 September 2023
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05431478.