Clinical trial · Interventional
Efficacy and Safety of Multimode Thermal Therapy in the Treatment of Early Peripheral Lung Cancer
NCT06453889CI-TRIAL-00077905not yet recruitingN/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 purpose of the study is to evaluate the efficacy and safety of multimode thermal therapy for early peripheral lung cancer, and to explore the changes of systemic immune microenvironment after multimode thermal therapy.
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 |
|---|---|---|---|
| Multimode thermal therapy | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Multimode thermal therapy
- description
- Percutaneous multimode thermal therapy
- interventionNames
- Device: Multimode thermal therapy
Primary outcomes (1)
- measure
- Complete ablation rate at 6 months post-procedure
- timeFrame
- 6 months
- description
- This refers to the proportion of completely ablated lesions in the total ablated lesions at 6 months after multimode thermal therapy.
Secondary outcomes (5)
- measure
- Complete ablation rate at 12 months post-procedure
- timeFrame
- 12 months
- description
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Age ≥18 years old; 2. Pathologically diagnosed as primary peripheral non-small cell lung cancer, preoperative staging suggested clinical staging as T1N0M0, stage IA (including new-onset lung cancer after surgery and multiple primary lung cancer); 3. The ECOG PS score is 0-2; 4. Expected survival ≥6 months; 5. Negative driver gene mutation: driver genes were defined as EGFR, ALK, ROS1, RET; 6. Agree to undergo multimode thermal therapy as initial treatment after being assessed unsuitable for surgery or refusing surgery, and sign informed consent. Exclusion Criteria: 1. Patients with poor cardiopulmonary function or other comorbidities who cannot tolerate multimode thermal therapy; 2. Patients whose chest CT indicated that the lung lesions could not be reached through the chest wall through multimode thermal therapy; 3. Severe liver and kidney function and coagulation function abnormalities, platelet count \<70×109/L; 4. Poor control of malignant pleural effusion; 5. Patients who have received other anti-tumor drugs or have used immune checkpoint inhibitors in the past 6 months; 6. The patient has an uncontrolled disease (including but not limited to active infection, symptomatic congestive heart failure, unstable angina, arrhythmia, mental illness, etc.); 7. Those who have undergone surgical operations or had allogeneic organ transplants within 1 month; 8. Primary immune deficiency or autoimmune diseases (e.g. rheumatoid arthritis, systemic lupus erythematosus, etc.); 9. Pregnant and lactating women; 10. Long-term use of steroid; 11. Other circumstances considered inappropriate for participation in this study.
References
Publications (0)
Data not yet available
No reference posted for this study.