The goal clinical trial is to evaluation of the safety and effectiveness of percutaneous and transbronchial argon-helium cryoablation in primary lung cancer and metastatic lung cancer. The main question it aims to answer are:Evaluation of the safety and effectiveness of percutaneous and transbronchial argon-helium cryoablation. Participants will undergo percutaneous or transbronchial argon-helium cryoablation.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
60
The participants would undergo Percutaneous or transbronchial argon-helium cryoablation.
Complete response rate and effective rate of target lesions
Enhanced imaging examination (CT, MRI or color Doppler ultrasound)
Time frame: during the operation of argon-helium cryoablation
Complete response rate and effective rate of target lesions
Enhanced imaging examination (CT, MRI or color Doppler ultrasound)
Time frame: 1 week after the operation of argon-helium cryoablation
Complete response rate and effective rate of target lesions
Enhanced imaging examination (CT, MRI or color Doppler ultrasound)
Time frame: 4 weeks(±7d) after the operation of argon-helium cryoablation
the iceball coverage rate during the procedure
CT
Time frame: during the procedure
Subjects' tolerance of the procedure
questionnaire
Time frame: 1 week after the operation of argon-helium cryoablation
the Eastern Cooperative Oncology Group Performance Status (ECOG PS) score
ECOG-PS questionnaire
Time frame: 4 weeks(±7d) after the operation of argon-helium cryoablation
To evaluate the operational performance of argon-helium cryoablation
questionnaire
Time frame: during the procedure
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