European Real-World Registry for Use of the Ion Endoluminal System
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorIntuitive Surgical
About this trial
The objective of this study is to collect collect real-world data for the Ion endoluminal system.
Eligibility criteria
Qualifiers
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.
Disqualifiers
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.
Trial design
Treatments tested in this trial
- Ion endoluminal system
Treatment groups
1,200 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov