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Clinical Trial

Safety and Efficacy of the Bi-Aspheric Monofocal IOL

NCT: NCT06380478 · COMPLETED

NCT IDNCT06380478
StatusCOMPLETED
Start Date2024-03-05
Completion2025-08-19

Brief 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.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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