Synapse 3D With Intravascular Indocyanine Green
Non-small Cell Lung Cancer, Primary Neoplasm
About this trial
This is an interventional treatment trial for Non-small Cell Lung Cancer focused on measuring Segmentectomy, Lung Cancer, Robotic Surgery, 3D Modelling, CT Imaging, Near-Infrared Fluorescence, IC-GREEN, Surgical Planning, Indocyanine Green, Early-Stage Lung Cancer, Surgical Mapping, Lung Preservation
Eligibility Criteria
Inclusion Criteria:
- Tumour size <3 cm
- Clinical Stage 1 Non-Small Cell Lung Cancer (NSCLC)
- CT-imaging confirming that the tumour is confined to one broncho-pulmonary segment, rendering the patient a candidate for segmental resection.
Exclusion Criteria:
- Hypersensitivity or allergy to ICG, sodium iodide, or iodine
- Women who are currently pregnant or breastfeeding; or women of childbearing potential who are not currently taking adequate birth control.
- Patients with clinical evidence of N1 or N2 disease on preoperative imaging
- Pulmonary Function tests demonstrating Forced Expiratory Volume in 1s (FEV1) or diffusion capacity of the lung for carbon monoxide (DLCO) less than or equal to 30% of predicted.
Sites / Locations
- St. Josephs Healthcare HamiltonRecruiting
Arms of the Study
Arm 1
Experimental
Synapse 3D Lung Modelling + IC-GREEN Segmentectomy
Patients within this arm will undergo a high-resolution CT scan of the chest, which is required by Synapse 3D to create accurate 3D virtual model reconstructions. At the start of the operation, the 3D virtual model of the segmental pulmonary anatomy will be displayed on the da Vinci Robotic platform for operative planning. The model will be used as a guide to determine which vessels are involved in the segment and need to be removed. The surgeon will ligate the pulmonary vein and pulmonary artery of the broncho-pulmonary segment with the lung cancer nodule, isolating it from any blood supply, and mark the proposed segmental planes based on the 3D model. ICG will be prepared as a sterile solution (2.5 mg/10mL) for injection. After vascular ligation, an 8 mL bolus of ICG solution will be injected into the peripheral vein catheter, followed by a 10 mL saline solution bolus