Lung Diseases Clinical Trial
Official title:
Post-Market Optimization Study of the EMPOWER® RF Catheter to Ablate Soft Tissue Lesions in the Lung
A post-market study to assess the performance and safety of a RF ablation catheter to bronchoscopically ablate lung lesions will be evaluated in patients with confirmed diagnosis of non-small cell lung cancer or metastatic lung lesions who are scheduled for surgical resection.
This study is a prospective, single-arm, multi-center, post-market study of bronchoscopic
radio frequency (RF) ablation treatment malignant lung lesions prior to surgical resection.
Up to 15 patients will be treated at the participating sites.
Patients identified for the study will have been scheduled for surgical resection as part of
their treatment for lung lesions. The RF ablation procedure will be performed during a
standard-of-care bronchoscopic procedure at minimum of 24 hours prior to resection. The
patients exits the study following surgical resection. The resected tissue will undergo
pathological evaluation for tissue viability.
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