N/A
Completed N=63
Comparative Clinical Evaluation of Daily Disposable Lenses in Symptomatic Daily Disposable Lens Wearers
Source: ClinicalTrials.gov NCT01035905 ↗Enrolled (actual)
63
Serious AEs
0.0%
Results posted
Oct 2010
Primary outcomePrimary: Lens Awareness — 8; 9 Participants
Summary
The purpose of this study is to evaluate the extent to which symptoms improve in symptomatic contact lens wearers when fit with one of two different daily disposable contact lenses.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Lens Awareness |
8; 9 | — |
Eligibility Criteria
Inclusion Criteria
- Currently wear daily disposable, spherical, soft lens wearers (except the two study products) for at least the past 6 months.
- Habitually wear lenses for at least 8 hours per day and 4 days per week.
- Report 2 or more qualifying symptoms with current contact lenses.
- Able to achieve visual acuity of at least 20/40 in each eye with habitual and with study lenses at dispense.
- Other protocol-defined inclusion/exclusion criteria may apply.
Exclusion Criteria
- Eye injury or surgery within twelve weeks immediately prior to enrollment.
- Currently enrolled in any clinical trial.
- Any use of ocular medications, exclusive of contact lens rewetting drops.
- History of corneal or refractive surgery.
- Cylinder correction greater than 1.00 D
- Current monovision contact lens wearers.
- Other protocol-defined inclusion/exclusion criteria may apply.
Data sourced from ClinicalTrials.gov (NCT01035905). 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.