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Trials / Recruiting

RecruitingNCT07158177

Clareon PanOptix Versus AcrySof PanOptix : Prospective Study Comparing Contrast Sensitivity

Clareon PanOptix Versus AcrySof PanOptix : Prospective Study Comparing Contrast Sensitivity. Study of Two Different Material of Intra Ocular Multifocal Lenses Aiming to Compare the Effect on Contrast Sensitivity.

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
Assistance Publique - Hôpitaux de Paris · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Retrospective, comparative, interventional, randomized, single-center study, contralateral (the patient's 2 eyes will be implanted: 1 CPO and the other APO) Patients presenting for cataract surgery with a request for presbyopia correction and managed as part of routine clinical practice. The main aim of the study is to demonstrate that contrast sensitivity is better with the Clareon PanOptix (CPO) intraocular lens (IOL) compared with the AcrySof PanOptix (APO) IOL 3 months after implantation.

Detailed description

Visit at Day3-10: usual follow-up visit, no additional examinations as part of the clinical investigation. Visit at 1 month: usual follow-up visit, no additional examinations as part of the clinical investigation. 3-month visit (end of clinical investigation): usual follow-up visit, plus contrast vision test and non-invasive aberrometry test (I-Trace) as part of the clinical investigation. Regarding a cataract surgery with a request for presbyopia, the protocol evaluate two differents devices (IOL intraocular lens).

Conditions

Interventions

TypeNameDescription
DEVICEAcrysof™ PanOptix™ toric or not, trifocal IOL CE marked, Alcon company.both of the patient's eyes will be implanted: 1 CPO and the other APO
DEVICEClareon Panoptixboth of the patient's eyes will be implanted: 1 CPO and the other APO

Timeline

Start date
2025-10-01
Primary completion
2026-10-15
Completion
2026-10-15
First posted
2025-09-05
Last updated
2026-03-30

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT07158177. Inclusion in this directory is not an endorsement.