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Clinical Trial Summary

The objective of the study is to evaluate the performance of the VERAFEYE System in subjects entitled to undergo a standard of care ablation or closure procedure. Results from this study will be used to guide development and refinement the VERAFEYE System. The study is not designed to collect data for product approval and as such does not have a safety or efficacy endpoint.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05931835
Study type Interventional
Source LUMA Vision Ltd.
Contact Elke Sommerijns, MSc
Phone +32479767156
Email elke.sommerijns@lumavision.com
Status Not yet recruiting
Phase N/A
Start date August 15, 2024
Completion date October 30, 2024

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