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UnknownNCT05416177

Assessment of Vivity With French Clinical Data Related to the Toric Model Study

Status
Unknown
Phase
Study type
Observational
Enrollment
31 (estimated)
Sponsor
Versailles Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Presbyopia-correcting implant (PC-IOL): AcrySof IQ Vivity (Alcon) has been evaluated in 2 large pivotal trials (US and OUS trials). These tests showed that this PC-IOL restored intermediate visual acuity (IVA) and near visual acuity (NV A) superior to that of the reference monofocal AcrySof implant. In these tests, it was demonstrated that distance visual acuity (DVA) was non-inferior. However, the intermediate visual acuity for this implant in its toric version has not been evaluated.

Conditions

Timeline

Start date
2022-09-01
Primary completion
2023-04-01
Completion
2023-07-01
First posted
2022-06-13
Last updated
2022-08-25

Source: ClinicalTrials.gov record NCT05416177. Inclusion in this directory is not an endorsement.

Assessment of Vivity With French Clinical Data Related to the Toric Model Study (NCT05416177) · Clinical Trials Directory