Pilot Evaluation of Two Multipurpose Solutions in Regards to Corneal Staining
Phase 4
Completed
- Conditions
- Corneal Staining
- Registration Number
- NCT00483795
- Lead Sponsor
- Innovative Medical
- Brief Summary
To evaluate corneal staining after contact lens instillation with two different multi purpose solutions.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- Not specified
Inclusion Criteria
- Patients 18 yrs or older
- Males or females
- Any race or ethnic background
- CL patients using (multipurpose solutions) MPS
- Patients using Acuvue 2 lenses
Exclusion Criteria
- Corneal refractive surgery within 6 months of this study.
- Contact lens use on day of examination.
- Corneal ectasia.
- Current use of Restasis
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method
- 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 underlie corneal staining caused by multipurpose contact lens solutions?
How do the formulations of the two multipurpose solutions in NCT00483795 compare to standard-of-care solutions in preventing corneal staining?
Are there specific biomarkers associated with increased risk of corneal staining in contact lens users?
What are the potential adverse events linked to multipurpose contact lens solutions and how are they managed clinically?
What alternative or combination therapies have been explored for mitigating corneal staining in contact lens wearers?
Trial Locations
- Locations (1)
Hazleton Eye Specialists
🇺🇸Hazleton, Pennsylvania, United States
Hazleton Eye Specialists🇺🇸Hazleton, Pennsylvania, United States