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Study identifier: NCT07164040 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Leica Microsystems Sponsored Study to Collect and Confirm Clinical Data on the Performance of the GLOW800 Device When Used in Accordance With Its Intended Use.

Condition: Reconstructive Surgical Procedures · Plastic Surgery · Vascular Surgical Procedure  ·  Sponsor: Leica Microsystems (Schweiz) AG

PhaseN/A
Planned participants29
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This post-market clinical follow-up (PMCF) study aims to confirm the safety and performance of the GLOW800 surgical microscope accessory when used in conjunction with the ARveo8x surgical microscope. The study evaluates fluorescence visualization and image quality during standard surgical procedures in the cerebral vascular area and plastic and reconstructive surgery. It is a non-interventional, observational study conducted in routine care settings across multiple European sites.

This description comes directly from the study's public registry record.

Talk to the study team

Daniela Leal  ·  +41793741989  ·  clinical.affairs@leica-microsystems.com

Always discuss trial participation with your own doctor first.

Locations (3)

Unidade Local de Saúde de São JoãoPorto, PortugalRecruiting
Hospital Germans Trias I PujolBarcelona, SpainNot Yet Recruiting
University Hospital BaselBasel, SwitzerlandNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT07164040