N/A
N=350
Comparative Performance of a Bausch & Lomb Multipurpose Solution and Alcon OptiFree Replenish Multipurpose Solution
Adverse Effect of Contact Lens Solution
Bottom Line
View on ClinicalTrials.gov: NCT00636194 ↗Enrolled (actual)
350
Serious AEs
0.0%
Results posted
Feb 2011
Primary outcome: Primary: Subjective Assessment of Comfort and Cleanliness — 89.71; 89.26; 87.45; 86.63 Scores on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Bausch & Lomb Multipurpose Solution (Device); Alcon OptiFree Replenish Multipurpose Solution (Device)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Bausch & Lomb Incorporated
- Primary completion
- Mar 2008
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Subjective Assessment of Comfort and Cleanliness |
89.71; 89.26; 87.45; 86.63; 82.98; 82.34 | — |
| SECONDARY Symptoms and Complaints |
85.4; 86.1; 79.2; 79.3; 87.0; 88.9 | — |
| SECONDARY Graded Slit Lamp Findings > Grade 2 |
0; 0; 0; 0; 3; 0 | — |
Summary
To evaluate the product performance of a Bausch & Lomb Multipurpose solution when compared to Alcon OptiFree Replenish Multipurpose Solution
Eligibility Criteria
Inclusion Criteria
- Subjects are adapted wearers of silicone hydrogel contact lenses
- VA correctable to 0.3 LogMAR or better (driving vision)
- Clear central cornea
- Subject uses a lens care system on a regular basis
Exclusion Criteria
- Systemic disease affecting ocular health
- Using systemic or topical medications
- wear a monovision, multifocal or toric contact lenses
- Any grade 2 or greater slit lamp findings
Data sourced from ClinicalTrials.gov (NCT00636194). 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.