Therapeutic Variables in Cataract Surgery
Phase 4
Completed
- Conditions
- Cataract Surgery
- Registration Number
- NCT00407017
- Lead Sponsor
- Innovative Medical
- Brief Summary
The purpose of this study is to compare patient outcomes in following cataract surgery in patients randomized to one of two surgical kits.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- Not specified
Inclusion Criteria
- Males or females scheduled to undergo cataract surgery
- Patients can be receiving monofocal IOLs only
- Likely to complete all study visits and able to provide informed consent
- Visual potential of 20/25 or better
Exclusion Criteria
- Known contraindications to any study medication or ingredients
- Active ocular diseases or uncontrolled systemic disease
- Active ocular allergies
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 are the key molecular mechanisms involved in cataract surgery outcomes with different surgical kits?
How does the surgical kit used in NCT00407017 compare to standard-of-care in terms of effectiveness and complication rates?
Are there specific biomarkers that predict better outcomes with one cataract surgical kit over another?
What adverse events are associated with the two surgical kits in NCT00407017 and how are they managed?
What are the current trends in cataract surgery technology and how does this trial contribute to the field?
Trial Locations
- Locations (1)
The Center for Excellence in Eye Care
🇺🇸Miami, Florida, United States
The Center for Excellence in Eye Care🇺🇸Miami, Florida, United States