The Clinical and Subjective Performance of Three Different MPDS With Silicon Hydrogel Lenses
Not Applicable
Completed
- Conditions
- Adverse Reaction to Contact Lens Solution
- Registration Number
- NCT01665612
- Lead Sponsor
- Finnsusp Ltd.
- Brief Summary
The purpose of the clinical investigation is to assess the clinical and subjective performance of three novel multipurpose disinfecting solutions (MPDS) in daily wear with two silicone hydrogel contact lenses (Lotrafilcon B and Comfilcon A).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
- age above 18
- experienced contact lens user
- good health (self-reported)
Exclusion Criteria
- eye disease or eye operations
- pregnancy
- medication that can affect sight
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Primary Outcome Measures
Name Time Method Clinical performance 1 month TBUT, conjunctival and limbal hyperemia, corneal vascularization, epithelial and stromal oedema, corneal infiltrates, endothelial regularity, corneal staining and papillar conjunctivitis
- Secondary Outcome Measures
Name Time Method Subjective performance 1 month E.g. Comfort
Trial Locations
- Locations (1)
Raision Näkökulma
🇫🇮Raisio, Finland
Raision Näkökulma🇫🇮Raisio, Finland