Comparative Study of the Wearing Satisfaction of Two Soft Contact Lens Designs.
Not Applicable
Completed
- Conditions
- Myopia
- Registration Number
- NCT00768885
- Lead Sponsor
- Bausch & Lomb Incorporated
- Brief Summary
To evaluate the wearing satisfaction of a new design of the PureVision soft contact lenses.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 64
Inclusion Criteria
- Subject is myopic
- Subjects who wear soft contact lenses that are exchanged at least biweekly at the time consent is obtained.
Exclusion Criteria
- Systemic disease affecting ocular health
- Using pharmaceuticals that may affect the function of the eyes or lenses.
- Subject possessing corneal infiltrate or corneal ulcers.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Primary Outcome Measures
Name Time Method Patient satisfaction 4 weeks
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms differentiate PureVision 1 and PureVision 2 contact lens designs for myopia correction?
How does the new PureVision lens design compare to standard soft contact lenses in terms of ocular comfort and visual acuity outcomes?
Are there specific biomarkers or patient characteristics that predict better wearing satisfaction with either PureVision 1 or PureVision 2 lenses?
What are the known adverse events associated with Bausch & Lomb PureVision soft contact lenses and how are they managed?
How do the hydrogel material properties of PureVision 1 and PureVision 2 impact tear film stability in myopic patients compared to competitor lens designs?
Trial Locations
- Locations (1)
Kodama Eye Clinic
🇯🇵Kyoto, Japan
Kodama Eye Clinic🇯🇵Kyoto, Japan