N/A
N=21
In-vivo Wettability Grading and Assessment Study
Myopia
Bottom Line
View on ClinicalTrials.gov: NCT01010555 ↗Enrolled (actual)
21
Serious AEs
0.0%
Results posted
May 2011
Primary outcome: Primary: On-eye Wettability — 1.33; 2.11; 1.70; 2.07 units on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- lotrafilcon B (Device); balafilcon A (Device); senofilcon A (Device); enfilcon A (Device)
- Age
- Pediatric, Adult, Older Adult · 17+ yrs
- Sex
- All
- Sponsor
- CIBA VISION
- Primary completion
- Apr 2010
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY On-eye Wettability |
1.33; 2.11; 1.70; 2.07 | — |
Summary
The purpose of this study is to investigate the front surface wettability of soft contact lenses while on eye.
Eligibility Criteria
Inclusion Criteria
- is at least 17 years of age
- has read and signed an information consent letter
- is a current daily wear contact lens wearer
- has acceptable fit with the study lenses
- has had an ocular exam in the last two years
- other protocol-defined inclusion criteria may apply
Exclusion Criteria
- has any ocular disease
- has undergone corneal refractive surgery or is aphakic
- has any systemic disease affecting ocular health
- is pregnant or lactating
- other protocol-defined exclusion criteria may apply
Data sourced from ClinicalTrials.gov (NCT01010555). 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.