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A Multicenter, Observational, Single Arm Study of the TECNIS Presbyopia-correcting Intraocular Lens

CompletedN/A

Sponsor: Johnson & Johnson Surgical Vision, Inc.

Conditions: Cataracts

Interventions: Intervention

Countries: Australia, Austria, France, Germany, India, Netherlands, South Korea, Spain

Ambispective post-market data collection on visual symptoms, patient satisfaction and surgeon experience with the TECNIS PC IOL.

Eligibility overview

Sex: ALL

Healthy volunteers: No

Study type: OBSERVATIONAL

Eligibility criteria

Inclusion Criteria:

* Patients who are bilaterally implanted with TECNIS PC IOL and are at least 45 days postoperative from their second eye surgery
* Clear intraocular media
* Signed informed consent and data protection documentation
* Availability, willingness, ability, and sufficient cognitive awareness to comply with examination procedures
* Ability to understand, read, and write English or the local language in which the informed consent and questionnaires are provided

Exclusion Criteria:

* Subjects with ongoing adverse events that might impact outcomes during the study
* Use of systemic or ocular medication that may affect vision
* Acute or chronic disease or condition, ocular trauma or surgery that may confound results
* Patients with amblyopia, strabismus, nystagmus
* Concurrent participation in another clinical trial

Locations (20)

Chatswood, New South Wales, Australia
Birtinya, Queensland, Australia
Woolloongabba, Queensland, Australia
Nedlands, Western Australia, Australia
Vienna, Austria
Brest, France
Marseille, France
Ahaus, Germany
Bonn, Germany
Bengaluru, India
Coimbatore, India
New Delhi, India
New Delhi, India
Rotterdam, Netherlands
Tilburg, Netherlands
Seoul, South Korea
Seoul, South Korea
Madrid, Spain
Madrid, Spain
Madrid, Spain