IRE Device
DeviceFor use in ablating soft tissue
Other names: The NanoKnife IRE device
NCT Number: NCT03769753
The purpose of this study is to test any good and bad side effects of surgery using IRE to treat cancer of the bile duct.
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Phase 2
Memoral Sloan Kettering Basking Ridge (Consent and Follow up), Basking Ridge, New Jersey, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
For use in ablating soft tissue
Other names: The NanoKnife IRE device
Time frame: within 30 days post-IRE
defined as CTCAE (version 5.0) grade 3 or higher complications
Memorial Sloan Kettering Cancer Center
Other
Trial Of IRE in Cholangiocarcinoma (TOnIC): Phase II
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07704021
Adenocarcinoma, Biliary Tract Diseases
Piacenza, PC, Italy
View Trial DetailsNCT05185947
Abdominal Neoplasms, Adenocarcinoma
Bethesda, Maryland, United States
View Trial DetailsNCT07619937
Adenocarcinoma, Carcinoma
Zhengzhou, Henan, China
View Trial DetailsNCT04572711
Adenocarcinoma, Biliary Stricture
Rochester, Minnesota, United States
View Trial Details