Biological treatment center in Fuda cancer hospital
Guangzhou, Guangdong, 510000, China
NCT Number: NCT02430753
The purpose of this study is to evaluate the safety and efficacy of irreversible electroporation (IRE) for Lung Neoplasms accompanied by Respiratory Function Insufficiency.
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Interventional
Not applicable
Guangzhou, Guangdong, 510000, China
By enrolling patients with Lung Neoplasms accompanied by Respiratory Function Insufficiency adapted to enrolled criteria, this study will document for the first time the safety and the short and long term efficacy of percutaneous IRE for Lung Neoplasms accompanied by Respiratory Function Insufficiency.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Irreversible Electroportion For Lung Neoplasms accompanied by Respiratory Function Insufficiency guide with ultrasound or/and CT.
Other names: NanoKnife
Time frame: 6 month
Time frame: 12 months
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
A minimum and maximum range of voltage for safe and effective IRE will be analyzed for optimal choice.
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 Lung Neoplasms Accompanied by Respiratory Function Insufficiency: Phase I and Phase II Clinical Trial
Acronym: IRE
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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