Clinical trial · Interventional
Evaluation of the Safety and Effectiveness of Percutaneous and Transbronchial Argon-helium Cryoablation
NCT05807022CI-TRIAL-00065445unknownN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Lung Cancer | Malignant Lung Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Percutaneous or transbronchial argon-helium cryoablation | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Percutaneous or transbronchial argon-helium cryoablation
- interventionNames
- Procedure: Percutaneous or transbronchial argon-helium cryoablation
Primary outcomes (3)
- measure
- Complete response rate and effective rate of target lesions
- timeFrame
- during the operation of argon-helium cryoablation
- description
- Enhanced imaging examination (CT, MRI or color Doppler ultrasound)
- measure
- Complete response rate and effective rate of target lesions
- timeFrame
- 1 week after the operation of argon-helium cryoablation
- description
- Enhanced imaging examination (CT, MRI or color Doppler ultrasound)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 90 Years
Show eligibility criteria text
Inclusion Criteria: * Primary or metastatic lung cancer with definite pathological diagnosis * Not suitable for thoracotomy due to serious or serious lung or systemic diseases * Peripheral lung cancer involves pleura and chest wall, and cannot be completely removed after surgery * There are indications for surgical resection, but the patient refuses to operate * Single tumor, maximum diameter ≤ 5cm * Or the number of tumors ≤ 3 and the maximum diameter ≤ 3cm * ECOG-PS score ≤ 2 * The expected survival period is more than three months * Those who have not participated in other clinical verifications within 3 months * Subjects voluntarily signed the informed consent form Exclusion Criteria: * Serious cardio-cerebral disease or other mental diseases * Severe pulmonary fibrosis, especially drug-induced pulmonary fibrosis * Patients with previous severe pulmonary dysfunction, pulmonary ventilation disorder and multiple pulmonary bullae * Have a history of immunodeficiency, including HIV test (enzyme-linked immunosorbent assay and Western blotting) positive * Chemotherapy, radiotherapy, interventional therapy, ablation and surgical treatment within 30 days before surgical treatment * There is a tendency to severe bleeding, and the platelet is less than 50 × 109/L and severe disorder of coagulation function * Coagulation index (PT, TT, APTT)\>2.5 times of the upper normal limit * Malignant pleural effusion on the same side of the ablation focus was not well controlled * Poor general condition, multiple organ failure, cachexia, severe anemia and nutritional metabolism disorder * Those who have extensive extrapulmonary metastasis and are not suitable for ablation treatment * Those who often use sedatives, sleeping pills, tranquilizers or other addictive drugs * Pregnant or lactating women * Those who can not judge the curative effect * Other conditions determined by the researcher to be unsuitable for the group, such as inability to tolerate cryoablation, difficulty in follow-up, and other serious diseases
References
Publications (0)
Data not yet available
No reference posted for this study.