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OpenTrials
Completed

NCT Number: NCT03769753

Trial of IRE in Cholangiocarcinoma

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Memoral Sloan Kettering Basking Ridge (Consent and Follow up), Basking Ridge, New Jersey, United States

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18 years or older
  • Capable of providing written and oral informed consent in English
  • Locally advanced disease based on preoperative work-up demonstrating that the tumor is unresectable due to portal vein, hepatic artery, and/or bile duct involvement, insufficient hypertrophy response of the future liver remnant after portal vein embolization, or patients not able to tolerate major liver surgery
  • Found to be unresectable intraoperatively based on vascular, biliary, or lymph node (N2) involvement upon exploratory laparotomy
  • Patients will be assessed for chemotherapy prior to treatment with IRE, but given the common problem of recurrent cholangitis, some patients will not be candidates for chemotherapy until after IRE is performed.

Exclusion criteria

  • Locally advanced PHC eligible and accepted for liver transplantation evaluation
  • PHC with > 5 cm extension along the common hepatic duct or common bile duct on preoperative imaging or intraoperative ultrasound
  • Metastases to peritoneum, liver or other organs confirmed by percutaneous biopsy, staging laparoscopy or intraoperative frozen section
  • Lymph node metastases beyond N2 stations, confirmed by intraoperative frozen sections or radiographic diagnosis
  • History of cardiac disease:
  • Congestive heart failure (NYHA class >2)
  • Active Coronary Artery Disease (defined as myocardial infarction within 6 months prior to screening)
  • Cardiac arrhythmias requiring anti-arrhythmic therapy or pacemaker (beta blockers are permitted)
  • Any implanted stimulation device (defined as implantable cardiac device and a pacemaker)
  • Uncontrolled hypertension (blood pressure must be ≤160/95 mmHg at the time of screening on a stable antihypertensive regimen)
  • Uncontrolled infections (> grade 2 NCI-CTC, version 3.0)
  • Epilepsy
  • Both narrowing (sclerosis) of the main portal vein and a reduced diameter of either the common hepatic artery, celiac trunk or superior mesenteric artery of >50%

Treatment and study plan

IRE Device

Device

For use in ablating soft tissue

Other names: The NanoKnife IRE device

Primary outcomes

  1. Number of Patients Experiencing a Clinically Relevant Complications

    Time frame: within 30 days post-IRE

    defined as CTCAE (version 5.0) grade 3 or higher complications

Sponsors and collaborators

Lead sponsor

Memorial Sloan Kettering Cancer Center

Other

Registry information

Official study title

Trial Of IRE in Cholangiocarcinoma (TOnIC): Phase II

Important dates

Study start
2018
Primary completion
2021
Study completion
2021
First posted
Dec 7, 2018
Registry last updated
Sep 10, 2022

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.

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