Clinical Trials Directory

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UnknownNCT04230629

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

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
Medical University of Vienna · Academic / Other
Sex
All
Age
40 Years
Healthy volunteers
Not accepted

Summary

On the day of surgery, the the eye with astigmatism of at least 0.75dpt receives a Vivinex XY1A , HOYA Surgical Optics GmbH and the second eye to be operated receives an XY1, HOYA Surgical Optics GmbH. A complete biomicroscopic examination and visual acuity testing using autorefractometer, will be performed 1 week (7-14days), 6 weeks (30-60days) and 5 month (4-6months) postoperatively.

Conditions

Interventions

TypeNameDescription
DEVICEVivinex XY1Implantation of an intraocular lens Hoya Vivinex XY1
DEVICEVivinex XY1AImplantation of an intraocular lens Hoya Vivinex XY1A

Timeline

Start date
2021-03-15
Primary completion
2021-12-30
Completion
2022-06-30
First posted
2020-01-18
Last updated
2021-03-09

Source: ClinicalTrials.gov record NCT04230629. Inclusion in this directory is not an endorsement.