N/A
N=196
Non-dispense Comfort Comparison of Two Silicone Hydrogel Lenses
Myopia
Bottom Line
View on ClinicalTrials.gov: NCT00808834 ↗Enrolled (actual)
196
Serious AEs
0.0%
Results posted
Oct 2010
Primary outcome: Primary: Comfort After Insertion — 8.7; 7.7 Scale 1-10
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Lotrafilcon A contact lens (Device); Senofilcon A contact lens (Device)
- Age
- Pediatric, Adult, Older Adult
- Sex
- All
- Sponsor
- CIBA VISION
- Primary completion
- Dec 2008
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Comfort After Insertion |
8.7; 7.7 | — |
Summary
The purpose of this study is to compare subjective responses to two contact lenses after 15 minutes of wear.
Eligibility Criteria
Inclusion Criteria
- Currently wearing soft contact lenses
- Replaces lenses on a weekly or longer schedule
- 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
- Currently wearing soft toric lens wearers
- Those who dispose of their soft lenses on a daily basis
- Other protocol-defined inclusion/exclusion criteria may apply
Data sourced from ClinicalTrials.gov (NCT00808834). 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.