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Clinical Trial Summary

This is an observational, single-center, non-control, open-label post-marketing study. Patients implanted with an aspicio™ Monofocal Intraocular Lens will be scheduled for a follow-up visit at least 3 months after the surgery to undergo a routine basic ophthalmological examination.


Clinical Trial Description

This is an observational, single-center, non-control, open-label post-marketing study. Patients implanted with an aspicio™ Monofocal Intraocular Lens will be scheduled for a single visit in the facilities of Chang Gung University Hospital at least 3 months after the surgery. Patients will undergo a routine basic ophthalmological examination. Additionally, and retrospectively, the patients' medical records will be reviewed to obtain information on visual acuity and adverse events at postoperative visit carried out 1 month after surgery. The data corresponding to the preoperative values of corneal curvature (flat meridian, curved meridian and axes), axial length measured by biometry, visual acuity and those corresponding to the implanted IOL will also be collected from the medical records. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06380478
Study type Observational
Source ICARES Medicus, Inc.
Contact Lisa Chen
Phone +88636579530
Email lisa.phchen@gmail.com
Status Recruiting
Phase
Start date March 5, 2024
Completion date December 25, 2024

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