Fuda Cancer Hospital
Guangzhou, Guangdong, 510665, China
NCT Number: NCT02333773
The purpose of this study is to evaluate the safety and efficacy of irreversible electroporation (IRE) for unresectable Portal venous tumor emboli.
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Interventional
Not applicable
Guangzhou, Guangdong, 510665, China
By enrolling patients with unresectable Portal venous tumor emboli adapted to enrolled criteria, this study will document for the first time the safety and the short and long term efficacy of percutaneous or intraoperative IRE for unresectable Portal venous tumor emboli.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Irreversible Electroportion For Unresectable Portal venous tumor emboli guide with ultrasound or/and CT.
Other names: NanoKnife
Time frame: 6 month
adverse effects
Time frame: 12 months
The primary objective of this project is to evaluate the efficacy (percentage of lesions that show no sign of recurrence 12 months after IRE)
Time frame: 3 months
A minimum and maximum range of voltage for safe and effective IRE will be analyzed for optimal choice.
Time frame: 12 months
Patients will be followed for 12 months after IRE for PFS assessing.
Time frame: 36 months
Patients will be followed for 36 months after IRE for OS analyzed.
Fuda Cancer Hospital, Guangzhou
Other
Irreversible Electroporation(IRE) For Unresectable Portal Venous Tumor Emboli: Phase I and Phase II Clinical Trial
Acronym: IRE
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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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