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N/A Completed N=60 Randomized Double-blind Treatment

Performance Assessment of a Modified Daily Disposable Contact Lens

Refractive Errors · Myopia · Hyperopia
Source: ClinicalTrials.gov NCT03762668 ↗
Enrolled (actual)
60
Serious AEs
0.0%
Results posted
Jan 2020
Primary outcomePrimary: High Contrast Distance Visual Acuity (logMAR) — -0.04; -0.04; -0.05; -0.05 logMar

Summary

The purpose of this study is to compare visual acuity between two daily disposable contact lenses.

Outcome Measures

OutcomeResultp-value
PRIMARY
High Contrast Distance Visual Acuity (logMAR)
-0.04; -0.04; -0.05; -0.05

Eligibility Criteria

Inclusion Criteria

  • Able to understand and sign an approved Informed Consent form;
  • Current wearer of commercial DAILIES TOTAL1 Contact Lenses in both eyes;
  • Other protocol-specified inclusion criteria may apply.

Exclusion Criteria

  • Any eye condition that contraindicates contact lens wear, as determined by the Investigator;
  • Any eye surgery that contraindicates contact lens wear, as determined by the Investigator;
  • Wears habitual contact lenses in an extended wear modality (routinely sleeping in lenses for at least 1 night per week)
  • Monocular (only one eye with functional vision);
  • Other protocol-specified exclusion criteria may apply.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03762668). 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.

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