Robotic-Assisted Bronchoscopy-Guided Synchronous Biopsy and Radiofrequency Ablation for Pulmonary Nodules

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-100
SponsorShanghai Chest Hospital

About this trial

This is a prospective, single-arm, open-label clinical study. The primary study objective is to evaluate the feasibility of synchronous biopsy and radiofrequency ablation for pulmonary nodules under robotic-assisted bronchoscopy.

Eligibility criteria

Qualifiers

Age ≥ 18 years old;

Chest CT indicates pulmonary nodules, highly suspected of being malignant;

Size of pulmonary nodules: 8 mm < maximum diameter ≤ 30 mm, and the number of pulmonary nodules requiring intervention ≤ 3;

Preoperative imaging evaluation indicates no clear lymph node metastasis or distant metastasis (cT1N0M0);

Disqualifiers

Patients who cannot tolerate general anesthesia due to advanced age or severe cardiopulmonary diseases, or other reasons;

The target nodule has been diagnosed as a malignant tumor or metastasis;

Patients with severe bleeding tendency or uncorrectable coagulation disorder (platelet count < 50×10^9 /L, prothrombin time > 18s, prothrombin activity < 40%);

Severe pulmonary fibrosis and pulmonary hypertension;

Trial design

Treatments tested in this trial

  • Robotic-assisted bronchoscopy-guided synchronous biopsy and radiofrequency ablation for pulmonary nodules

Treatment groups

76 Participants
are divided into 1 treatment group

Sponsors and collaborators