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Intraocular Lens
Treatment Group 1 for Cataract
N/A
Waitlist Available
Led By Steven J Dell, MD
Research Sponsored by Dell Laser Consultants
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 90 days post-operative
Awards & highlights
Study Summary
The objective of this study is to evaluate the uncorrected binocular distance, intermediate, and near visual acuities, and assess patient's spectacle independence and satisfaction in individuals undergoing bilateral cataract extraction that have received two different arms of near add design IOLs of the same diffractive multifocal model.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 90 days post-operative
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~90 days post-operative
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Measurements of uncorrected and best corrected visual acuities under mesopic illumination at distance, intermediate, and near using the ETDRS chart.
Trial Design
2Treatment groups
Active Control
Group I: Treatment Group 1Active Control1 Intervention
50 qualified study patients will receive the +2.75D (ZKB00) in their dominant eye and the +3.25D (ZLB00) in their non-dominant eye.
Group II: Treatment Group 2Active Control1 Intervention
50 qualified study patients will receive the +2.75D (ZKB00) in their dominant eye and the +4.00D (ZMB00) in their non-dominant eye.
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Who is running the clinical trial?
Dell Laser ConsultantsLead Sponsor
Abbott Medical OpticsIndustry Sponsor
44 Previous Clinical Trials
6,693 Total Patients Enrolled
23 Trials studying Cataract
4,567 Patients Enrolled for Cataract
Steven J Dell, MDPrincipal InvestigatorDell Laser Consultants
1 Previous Clinical Trials
88 Total Patients Enrolled
Frequently Asked Questions
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