cryotherapy
ProcedureAfter entering the group subject receive Cryotherapy on lung cancer
Other names: Cryoablation
NCT Number: NCT02744664
This trial is to designed to assess the efficacy and safety of Cryotherapy combine with Icotinib for Advanced NSCLC Patients harboring EGFR mutation.
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Notify Me18 year–75 year
All sexes
Interventional
Phase 4
In this single arm clinical study, enrolled patients, with advanced stage NSCLC and confirmed epidermal growth factor receptor (EGFR) mutation, would receive cryotherapy for tumors and begin Icotinib, an EGFR tyrosine kinase inhibitor administration thereafter. Progression free survival, overall survival and safety wil be observed.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
After entering the group subject receive Cryotherapy on lung cancer
Other names: Cryoablation
After Cryotherapy, subjects begin Icotinib administration
Other names: EGFR-TKI
Time frame: 2.5 years
the time that subjects reach their disease progress
Time frame: 3-3.5 years
the time subjects die
Fuda Cancer Hospital, Guangzhou
Other
A Single Arm, Open Label, Perspective Study to Determine the Efficacy and Safety of Icotinib Combine Cryotherapy for Advanced NSCLC Patients
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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