N/A
N=60
Performance Assessment of a Modified Daily Disposable Contact Lens
Refractive Errors · Myopia · Hyperopia
Bottom Line
View on ClinicalTrials.gov: NCT03762668 ↗Enrolled (actual)
60
Serious AEs
0.0%
Results posted
Jan 2020
Primary outcome: Primary: High Contrast Distance Visual Acuity (logMAR) — -0.04; -0.04; -0.05; -0.05 logMar
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Modified delefilcon A contact lenses (Device); Delefilcon A contact lenses (Device)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Alcon Research
- Primary completion
- Jan 2019
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY High Contrast Distance Visual Acuity (logMAR) |
-0.04; -0.04; -0.05; -0.05 | — |
Summary
The purpose of this study is to compare visual acuity between two daily disposable contact lenses.
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.
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.