Clinical Investigation of Patient Outcomes after IOL Implantation with Different IOL Delivery Systems
Not Applicable
- Conditions
- H26.9Cataract, unspecified
- Registration Number
- DRKS00020134
- Lead Sponsor
- Alcon Research, LLC
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 24
Inclusion Criteria
Adults, 22 years of age or older, diagnosed with bilateral cataracts grades
- Planned small incision cataract removal surgery
- Preoperative corneal astigmatism < 1.50 D in both eyes
Other protocol-defined inclusion criteria may apply.
Exclusion Criteria
- Previous or planned refractive surgery during the subject’s participation in the study
- Previous corneal transplant
- Rubella, congenital, traumatic, or complicated
- Any subject currently participating in another investigational drug or device study that may confound the results of this investigation.
Other protocol-defined exclusion criteria may apply.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Mean monocular distance BCDVA at 1 month after cataract surgery.
- Secondary Outcome Measures
Name Time Method ot Applicable