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Remote Augmented Reality Technical Support During Catheter Ablation for Atrial Fibrillation

Tests remote headset-based technical support during ablation in adults with atrial fibrillation.

Plain-language title generated from the registry record
Registry title: Augmented Reality Aided Remote Access and Technical Support for Complex Ablation Procedures

Key facts

Where
Lübeck, GermanySee the site

Where in Germany

  • University Hospital Schleswig-HolsteinLübeck, GermanyNo longer taking part

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Trial details

Who runs it
University of Luebeck
Trial code
NCT07777042
Record updated
20 August 2026
Original description
Prospective, randomized, controlled, single-center pilot study evaluating the feasibility and safety of augmented reality-based remote technical support using the Microsoft HoloLens and EnSite™ Connected Care compared with conventional on-site support during 3D electroanatomical mapping-guided electrophysiological procedures. The study also assesses the feasibility of an AI-based algorithm integrated into the Medinbox Link system for automated procedural report generation and detection of protocol deviations from standard clinical practice.Read full original descriptionShow less

Augmented Reality Aided Remote Access and tecHnical suppOrt for compLex ablatiOn Procedures

Prospective, randomized, controlled, single-center pilot study evaluating the feasibility and safety of augmented reality-based remote technical support using the Microsoft HoloLens and EnSite™ Connected Care compared with conventional on-site support during 3D electroanatomical mapping-guided electrophysiological procedures. The study also assesses the feasibility of an AI-based algorithm integrated into the Medinbox Link system for automated procedural report generation and detection of protocol deviations from standard clinical practice.

Inclusion: Patients age ≥ 18 years; Indication for 3D electroanatomical mapping-based catheter ablation for the treatment of AF; Signed written informed consent.

Exclusion: Patient is unable or unwilling to provide informed consent; Patient is included in another randomised clinical trial; Inability to comply with the study procedures.

ClinicalTrials.gov NCT07777042