Non-small Cell Lung Cancer Clinical Trial
Official title:
Synapse 3D With Intravascular Indocyanine Green Fluorescence Mapping for Targeted Pulmonary Segmental Resection Trial: A Phase I Safety and Feasibility Trial
With the advent of CT screening for lung cancer, an increasing number of NSCLCs are being detected at very early stages, and the demand for pulmonary segmentectomy is rising rapidly. As such, there is a need to develop new surgical techniques to facilitate minimally invasive pulmonary segmentectomy, as segmentectomy may provide a number of significant advantages over lobectomy for patients presenting with early-stage lung cancer, or for patients unable to undergo a full lobectomy due to existing comorbidities. This study will provide the first case series using preoperative 3D anatomical planning (Synapse 3D) added to ICG and NIF-guided robotic segmentectomy to date and will be the first reported use of Synapse 3D-guided targeted pulmonary segmental resection in Canada. As lung cancer is the most frequently fatal cancer in North America, many thousands of patients will be able to benefit from this operation every year.
Status | Recruiting |
Enrollment | 32 |
Est. completion date | December 31, 2024 |
Est. primary completion date | September 30, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | 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. |
Country | Name | City | State |
---|---|---|---|
Canada | St. Josephs Healthcare Hamilton | Hamilton | Ontario |
Lead Sponsor | Collaborator |
---|---|
St. Joseph's Healthcare Hamilton |
Canada,
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Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Segmental Resection Conversion Rate | Rate of conversions to lobectomy will be measured by collecting the proportion of conversions to lobectomy. | 1 year | |
Primary | Number of Participants with Post Operative Complications | Post operative complications will be reported and measured using the Ottawa Thoracic Morbidity and Mortality Classification of (a) Adverse reactions to ICG dye at the time of surgery and (b) Perioperative complications through study completion. | 1 year | |
Secondary | Anatomical Accuracy of the 3D Lung Model | Anatomical accuracy will be evaluated using the criteria listed in points a-c. A score of 3/3 on these items will indicate success of anatomical accuracy
Ex-vivo localization of lesions; Ex-vivo confirmation of tumor-free margins around lesion; Ex-vivo confirmation of adequate anatomical inter-segmental. |
1 year | |
Secondary | Surgeon Confidence | A pre-operative CT scan based, a pre-operative 3D reconstruction based and post segmental resection surgeon confidence score will be obtained on a scale of 1-5:
1 - not at all confident, 2 - somewhat confident, 3 - confident, 4 - very confident, 5 - extremely confident. |
1 year | |
Secondary | Operation Time | Length of time of the operation will be measured by collecting the time the patient entered the operating room until the time the patient left the operating room. | 1 year | |
Secondary | Conversion to Thoracotomy | Rate of conversion to thoracotomy will be measured by collecting the proportion of conversions to thoracotomy. Descriptive analysis of reasons for conversion will also be collected. | 1 year | |
Secondary | Chest Tube Duration | Duration the patient had chest tubes in situ will be measured by collecting the date of surgery and the date the chest tube was removed. | 1 year | |
Secondary | Length of Stay | Duration of hospital length of stay will be measured by collecting the data of admission and the date of discharge. | 1 year | |
Secondary | Estimated Blood Loss | Estimated blood loss will be measured at the time of operation by OR staff. | 1 year |
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