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)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06923774
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