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
24 participants
OBSERVATIONAL
2019-12-12
2022-09-13
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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trifocal intraocular lens
Alcon Trifocal and Trifocal Toric Intraocular Lenses
Panoptix Model #TFAT00 for the UV Absorbing Trifocal IOL. Torics:
TFAT30, TFAT40, TFAT50, TFAT60
Interventions
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Alcon Trifocal and Trifocal Toric Intraocular Lenses
Panoptix Model #TFAT00 for the UV Absorbing Trifocal IOL. Torics:
TFAT30, TFAT40, TFAT50, TFAT60
Eligibility Criteria
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Inclusion Criteria
* Visually significant cataract
* Potential post-operative visual acuity of 20/25 or better
* Age 18 years or older
Exclusion Criteria
* Irregular astigmatism
* Prior corneal refractive surgery
18 Years
ALL
No
Sponsors
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Alcon Research
INDUSTRY
Weill Medical College of Cornell University
OTHER
Responsible Party
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Principal Investigators
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Ashley Brissette, MD
Role: PRINCIPAL_INVESTIGATOR
Weill Medical College of Cornell University
Locations
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Weill Cornell Medicine
New York, New York, United States
Countries
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Other Identifiers
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19-05020251
Identifier Type: -
Identifier Source: org_study_id
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