N/A
Completed N=22
Evaluation of Silicone Hydrogel Lens Wettability With Marketed Lens Care Solutions
Contact Lens Wear
Source: ClinicalTrials.gov NCT01252134 ↗
Enrolled (actual)
22
Serious AEs
0.0%
Results posted
Jun 2012
Primary outcomePrimary: Ex Vivo Contact Angle — 104.8; 104.9; 103.3 degrees
Summary
The purpose of this study is to assess ex vivo wettability of a commonly prescribed silicone hydrogel (SiH) contact lens with three marketed contact lens care solutions.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Ex Vivo Contact Angle |
104.8; 104.9; 103.3 | — |
| SECONDARY Subjective Comfort |
87.3; 87.3; 86.4 | — |
| SECONDARY Corneal Staining Type |
5.4; 8.8; 3.0 | — |
| SECONDARY Corneal Staining Extent |
0.7; 3.1; 0.9 | — |
Eligibility Criteria
Inclusion Criteria
- 18 years of age
- Soft contact lens wear on a daily wear basis
- Able to wear lenses at least 8 hours
- Generally healthy with normal ocular health
- Other protocol-defined inclusion criteria may apply
Exclusion Criteria
- Use of additional lens cleaners
- Known sensitivities to any ingredient in any of the study products
- History of ocular surgery/trauma within the last 6 months
- Other protocol-defined exclusion criteria may apply
Data sourced from ClinicalTrials.gov (NCT01252134). 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.