A European Multi-Center, Prospective, Single-Arm, Observational Study to Evaluate Real-World Outcomes for the Ion Endoluminal System
Status: Recruiting
Location: See all (4) locations...
Intervention Type: Device
Study Type: Observational
SUMMARY
The objective of this study is to collect collect real-world data for the Ion endoluminal system.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:
• 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.
Locations
Other Locations
France
Hôpital Marie Lannelongue
NOT_YET_RECRUITING
Le Plessis-robinson
Switzerland
Universitätsspital Zürich
RECRUITING
Zurich
United Kingdom
University College London Hospitals NHS Foundation Trust
NOT_YET_RECRUITING
London
Wythenshawe Hospital, Manchester University NHS Foundation Trust
NOT_YET_RECRUITING
Manchester
Contact Information
Primary
Jana Meschede
IonEURegistry@intusurg.com
+41 21 821 2000
Backup
Martha Bean
IonEURegistry@intusurg.com
+41 21 821 2000
Time Frame
Start Date: 2025-09-10
Estimated Completion Date: 2029-10
Participants
Target number of participants: 1200
Treatments
Observation Group
Subjects with biopsy and/or localization of lung nodule(s)
Related Therapeutic Areas
Sponsors
Leads: Intuitive Surgical