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

NCT06923774

RecruitingN/A

Sponsor: Intuitive Surgical

Conditions: Pulmonary Nodule, Lung Cancer

Interventions: Ion endoluminal system

Countries: France, Germany, Switzerland, United Kingdom

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

Eligibility overview

Sex: ALL

Age: 18 Years to —

Healthy volunteers: No

Study type: OBSERVATIONAL

Eligibility criteria

Inclusion Criteria:

* 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 Criteria:

* 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.

Locations (7)

Le Plessis-Robinson, France
Berlin, Germany
Hemer, Germany
Wiesbaden, Germany
Zurich, Switzerland
London, United Kingdom
Manchester, United Kingdom