Last updated on June 2019

AcrySof Toric IQ Post-Market Clinical Study


Brief description of study

The purpose of this study is to clinically confirm the rotational stability of a modified AcrySof IQ toric intraocular lens (IOL) in a Japanese population.

Detailed Study Description

Patients will be examined pre-operatively to up to 3 years post-operatively. One eligible eye will be selected as a target eye for efficacy analysis. If both eyes are eligible, the eye in which the IOL is implanted first will be selected as the target eye.

Clinical Study Identifier: NCT03350503

Recruitment Status: Closed


Brief Description Eligibility Contact Research Team


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