N/A
N=59
Daily Wear Comparison of Enhanced and Non-Enhanced Silicone Hydrogel Lenses
Myopia
Bottom Line
View on ClinicalTrials.gov: NCT00813982 ↗Enrolled (actual)
59
Serious AEs
0.0%
Results posted
Oct 2010
Primary outcome: Primary: Overall Vision — 8.7; 8.7 Units on a Scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Lotrafilcon A Experimental Contact Lens (Device); Lotrafilcon A Commercial Contact Lens (Device)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- CIBA VISION
- Primary completion
- Dec 2008
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Overall Vision |
8.7; 8.7 | — |
Summary
The purpose of this study is to compare an experimental contact lens with a currently marketed contact lens.
Eligibility Criteria
Inclusion Criteria
- Able to wear contact lenses for a minimum of 5 days a week, at least 8 hours a day
- On exam have ocular findings that are considered normal and would not prevent the safe wear of contact lenses
- Other protocol-defined inclusion/exclusion criteria may apply
Exclusion Criteria
- Requires concurrent ocular medication
- Eye injury or surgery within twelve weeks immediately prior to enrollment
- Evidence of systemic or ocular abnormality, infection, or disease likely to affect successful wear of contact lenses or use of their accessory solutions
- Any active corneal infection
- Any use of medications for which contact lens wear would be contraindicated
- History of corneal refractive surgery
- Wears toric contact lenses
- Other protocol-defined inclusion/exclusion criteria may apply
Data sourced from ClinicalTrials.gov (NCT00813982). 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.