RecruitingNCT06923774

European Real-World Registry for Use of the Ion Endoluminal System

A European Multi-Center, Prospective, Single-Arm, Observational Study to Evaluate Real-World Outcomes for the Ion Endoluminal System


Sponsor

Intuitive Surgical

Enrollment

1,200 participants

Start Date

Sep 9, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

The objective of this study is to collect collect real-world data for the Ion endoluminal system.


Eligibility

Min Age: 18 Years

Inclusion Criteria3

  • Patient is aged 18 years or older at time of consent.
  • Patient is planned to undergo a lung lesion biopsy(s) and/or localization procedure(s) utilizing the Ion endoluminal system.
  • Patient is willing and able to give written informed consent for clinical study participation.

Exclusion Criteria5

  • Patient is participating in an interventional research study or research study with investigational agents with an unknown safety profile that would interfere with participation in this study or study results.
  • Female patient that is pregnant or breast feeding as determined by standard site practices.
  • Patient is legally incapacitated or in a legal/court ordered institution or is part of a known vulnerable population, including but not limited to dependency on the sponsor, hospital or study doctor.
  • Patient is not willing to comply with post-procedure study participation requirements.
  • Investigator, in their professional opinion, has decided that it is in the patient's best interest to not participate in the clinical study.

Interventions

DEVICEIon endoluminal system

Lung nodule biopsy and/or localization procedure using the Ion endoluminal system per sites' standard of care


Locations(5)

Hôpital Marie Lannelongue

Le Plessis-Robinson, France

Helios Klinikum Emil von Behring

Berlin, Germany

Universitätsspital Zürich

Zurich, Switzerland

University College London Hospitals NHS Foundation Trust

London, United Kingdom

Wythenshawe Hospital, Manchester University NHS Foundation Trust

Manchester, United Kingdom

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06923774


Related Trials