About this trial
Using RBS as the navigation and treatment platform, precisely navigate to the target lesion. Utilize r-EUBS and nCLE to identify the lesion, and when the confocal AI model recognizes the lesion as malignant, perform a biopsy. Subsequently, under the guidance of OBCT, carry out ablation treatment of the lesion.
Eligibility criteria
Qualifiers
Age ≥18 years, male or female.
High-risk pulmonary nodule/tumor maximum diameter ≤3 cm.
Lesion judged suitable for bronchial navigation-guided diagnosis and treatment.
Ineligible for surgery or refuses surgery/radiotherapy; agrees to primary ablation therapy; provides written informed consent.
Disqualifiers
Diffuse bilateral lung lesions unresponsive to ablation.
Contraindication to bronchoscopy or inability to tolerate/cooperate with bronchoscopy.
Severe bleeding tendency or irreversible coagulopathy (PT >18 s, PTA <40%).Platelet count <70×10⁹/L; anticoagulant/antiplatelet therapy discontinued <1 week before ablation (except prophylactic low-molecular-weight heparin).
Severe pulmonary impairment (maximal voluntary ventilation <40%).
Trial design
Treatments tested in this trial
- Ablation