Clinical trial · Interventional
Efficacy and Safety Study of Medical Thoracoscope Cryotherapy Combined Standard First-line Treatment of Advanced Non-small Cell Lung Cancer and Malignant Pleural Effusion
The Efficacy and Safety Study of Medical Thoracoscope Cryotherapy Combined With Standard First-line Treatment of Advanced Non-small Cell Lung Cancer and Malignant Pleural Effusion: a Multicenter, Prospective, Randomized, Controlled Clinical Trial
- 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)
This study intends to investigate the efficacy and safety of medical thoracoscopic cryotherapy combined with standard first-line treatment of advanced non-small cell lung cancer with malignant pleural effusion through a randomized controlled clinical trial.
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 |
|---|---|---|---|
| Non Small Cell Lung Cancer | Lung Non-Small Cell Carcinoma | ALIAS | 0.90 |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Medical thoracoscopic cryotherapy combined with standard first-line therapy for advanced non-cell lung cancer | Other | — | UNRESOLVED |
| Sequential intrathoracic injection of cisplatin/erythromycin combined with standard first-line therapy for advanced non-cell lung cancer | Other | — | UNRESOLVED |
| Standard first-line therapy for advanced non-cell lung cancer without intrathoracic treatment | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (3)
- type
- EXPERIMENTAL
- label
- Experimental group (medical thoracoscopic cryotherapy)
- interventionNames
- Other: Medical thoracoscopic cryotherapy combined with standard first-line therapy for advanced non-cell lung cancer
- type
- ACTIVE_COMPARATOR
- label
- Cisplatin/erythromycin control group (sequential intrathoracic injection of cisplatin/erythromycin)
- interventionNames
- Other: Sequential intrathoracic injection of cisplatin/erythromycin combined with standard first-line therapy for advanced non-cell lung cancer
- type
- OTHER
- label
- Blank control group
- description
- Only intrathoracic tube was used to drain pleural effusion, and local pleural cavity was not treated.
- interventionNames
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: 1. 18-75 years old; 2. Non-small cell lung cancer with pleural metastasis confirmed by histopathology or cytology; 3. ECOG score 0-1; 4. Cardiopulmonary function can tolerate painless thoracoscopic examination; 5. Patients who underwent medical thoracoscopy for pleural effusion at first diagnosis and underwent medical thoracoscopy cryotherapy at the same time of biopsy were also included in the study. Non-small cell lung cancer was confirmed by pathological results; 6. All subjects or their guardians must sign the informed consent before entering the study. Exclusion Criteria: 1. Expected survival \<2 months; 2. Hemoglobin \<110g/L, white blood cell count \<3×109/L, neutrophil \<2.0×109/L, platelet \<100×109/L; 3. severe cardiac insufficiency, abnormal liver and kidney function (blood test results of transaminase and creatinine \> 1.5 times the normal upper limit); 4. have received chemotherapy or anti-angiogenic drugs (such as bevacizumab, endu, anlotinib, etc.); 5. History of radiotherapy; 6. history of intrathoracic local treatment; 7. multiple serous cavity effusion, or bilateral pleural effusion; 8. patients allergic to erythromycin; 9. the lung cannot be reopened.
References
Publications (0)
Data not yet available