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User Acceptability Evaluation of Pseudophakic Patients Previously Implanted With the TECNIS Odyssey IOL

NCT06005675•Johnson & Johnson Surgical Vision, Inc.

View on ClinicalTrials.gov

Summary

Prospective collection of data from medical records, multicenter, post-market clinical follow-up study.

Eligibility

Age

All ages

Sex

ALL

Healthy Volunteers

Inclusion Criteria

•1. Previously bilaterally implanted with TECNIS Odyssey IOL, following cataract extraction;
•2. Enrollment at least 21 days after second eye surgery;
•3. Clear intraocular media in each eye;
•4. Signed informed consent and data protection documentation necessary to comply with applicable privacy laws pertaining to medical treatment in the governing countries;
•5. Availability, willingness, ability, and sufficient cognitive awareness to comply with examination procedures;
•6. Ability to understand, read, and write in English

Exclusion Criteria

•1. Concurrent participation in an interventional clinical trial during the time from which the data will be collected;
•2. Use of systemic or ocular medication that may affect vision
•3. Prior corneal refractive surgery in each eye (i.e., LASIK, PRK, SMILE, RK, CK); NOTE: Limbal relaxing incisions (LRI) are permissible as planned at the time of surgery (intraoperatively) but not postoperatively until after completion of the study visits;
•4. Ongoing adverse events that might impact study measurements, as determined by the investigator;
•5. Acute or chronic disease or condition, ocular trauma, or surgery that may confound study measurements (e.g., clinically significant macular degeneration, glaucoma, cystoid macular edema, proliferative diabetic retinopathy, keratoconus, etc.);
•6. Amblyopia, strabismus, nystagmus in each eye

Locations (4)

Empire Eye and Laser Center

Bakersfield, California, United States

Center For Sight

Venice, Florida, United States

Waring Vision Institute

Mt. Pleasant, South Carolina, United States

Vance Thompson Vision

Sioux Falls, South Dakota, United States

Key Dates

Start Date

September 6, 2023

Primary Completion Date

May 1, 2024

Completion Date

May 1, 2024

Last Updated

April 25, 2025

Enrollment

ACTUAL participants

Conditions

Cataracts

Interventions

Intervention

DEVICE

Rotation of Hydrophobic Acrylic Lenses - Rayner RA0800C & Alcon Clareon & Hoya Nanex & Hoya Vivinex XY1-EM & RayOne EMV Toric & PODEYE Toric

NCT03803852

Age Related CataractsAstigmatism

View study

RECRUITING

Congenital Muscle Disease Study of Patient and Family Reported Medical Information

NCT01403402

Congenital Muscular Dystrophy With ITGA7 (Integrin Alpha-7) DeficiencyAlpha-Dystroglycanopathy (Congenital Muscular Dystrophy and Abnormal Glycosylation of Dystroglycan With Severe Epilepsy)+50 more

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: April 25, 2025Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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User Acceptability Evaluation of Pseudophakic Patients Previously Implanted With the TECNIS Odyssey IOL

Inclusion Criteria

Exclusion Criteria

Rotation of Hydrophobic Acrylic Lenses - Rayner RA0800C & Alcon Clareon & Hoya Nanex & Hoya Vivinex XY1-EM & RayOne EMV Toric & PODEYE Toric

Congenital Muscle Disease Study of Patient and Family Reported Medical Information

A Post-market Clinical Study to Collect Safety and Performance Data on Johnson & Johnson Surgical Vision Products

Clinical Results of a Monofocal Aspheric Bitoric Intraocular Lens With Plate Haptics in Hyperopic Eyes (HIPER-AT-TORBI)

Evaluation of Real-World Data on the Performance of the TECNIS Odyssey™ IOL

Evaluation of Physiological Responses at the Anterior Surface of Two (Hydrophobic Acrylic) Intraocular Lens Models