Patient Satisfaction in Post-LASIK Patients With Presbyopia-Correcting IOLs vs. Post-Lasik Patients With Monofocal IOLs
NCT ID: NCT04134507
Last Updated: 2020-12-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
44 participants
OBSERVATIONAL
2019-10-25
2020-12-01
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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COHORT
OTHER
Study Groups
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Extended Depth of Focus IOL
Post-LASIK patients with implantation of a presbyopia-correcting IOL
No interventions assigned to this group
Monofocal IOL
Post-LASIK patients with implantation of a monofocal IOL
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Post cataract surgery
* Implantation of ZLB00, ZXR or ZXT, ZCB00, or AO60 intraocular lenses
* Spherical values greater than ± 0.50 and/or cylinder magnitude greater than 0.75D
Exclusion Criteria
* Any newly acquired ocular condition or pathology (e.g., ARMD, epiretinal membrane, chronic dry eye, irregular astigmatism, diabetic retinopathy)
* Max sphere no greater than ± 0.50D and cylinder less than and/or equal to 0.75D
ALL
Yes
Sponsors
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Bucci Laser Vision Institute
OTHER
Responsible Party
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Locations
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Bucci Laser Vision
Wilkes-Barre, Pennsylvania, United States
Countries
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References
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Bucci FA Jr. Patient Satisfaction, Visual Outcomes, and Regression Analysis in Post-LASIK Patients Implanted With Multifocal, EDOF, or Monofocal IOLs. Eye Contact Lens. 2023 Apr 1;49(4):160-167. doi: 10.1097/ICL.0000000000000979. Epub 2023 Feb 22.
Other Identifiers
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FAB-USA-001
Identifier Type: -
Identifier Source: org_study_id