N/A
Completed N=22
Clinical Comparison of Two Daily Disposable Soft Contact Lenses
Myopia · Refractive Errors
Source: ClinicalTrials.gov NCT03518008 ↗
Enrolled (actual)
22
Serious AEs
0.0%
Results posted
Apr 2019
Primary outcomePrimary: Overall Quality of Vision — 9.2; 8.6 units on a scale
Summary
The purpose of this study is to evaluate the overall performance of investigational contact lenses (DD T2) when compared to clariti® 1 day contact lenses.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Overall Quality of Vision |
9.2; 8.6 | — |
Eligibility Criteria
Inclusion Criteria
- Understand and sign an Informed Consent Form;
- Successful wear of daily disposable 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) 20/25 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.
Exclusion Criteria
- Anterior segment infection, inflammation, or abnormality or disease that contraindicates contact lens wear, as determined by the Investigator;
- Use of systemic or ocular medications for which contact lens wear could be contraindicated, as determined by the Investigator;
- Refractive, ocular, or intraocular surgery, as specified in the protocol;
- Eye condition or injury, as specified in the protocol;
- Current or history of intolerance, hypersensitivity, or allergy to any component of the study products;
- Wearing habitual contact lenses in an extended wear modality (routinely sleeping in lenses for at least 1 night per week) over the last 3 months prior to enrollment;
- Use of topical ocular medications and artificial tear or rewetting drops requiring instillation during contact lens wear;
- Currently wearing clariti® 1 day contact lenses;
- Habitually wearing monovision or multifocal lenses during the last 3 months;
- Other protocol-specified exclusion criteria may apply.
Data sourced from ClinicalTrials.gov (NCT03518008). 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.