3D VR and Indocyanine Green for Pulmonary Segmental Resection in NSCLC
3-Dimensional VR Modelling (Elucis) with Intravascular Indocyanine Green Fluorescence Mapping
+ 3-Dimensional Modelling (Synapse 3D) with Intravascular Indocyanine Green Fluorescence Mapping
Bronchial Neoplasms+7
+ Carcinoma, Bronchogenic
+ Carcinoma, Non-Small-Cell Lung
Treatment Study
Summary
Study start date: December 1, 2026
Actual date on which the first participant was enrolled.This clinical trial is focused on improving a surgical technique called segmental resection for patients with early-stage non-small cell lung cancer (NSCLC). Typically, this type of surgery is very challenging due to the complex and varying anatomy of the lungs. It is difficult for surgeons to clearly see and separate the different parts of the lung during the operation. The current success rate for completing this surgery is about 60%, which is quite low. The study aims to enhance this procedure using 3-dimensional virtual reality (VR) modelling to help plan and conduct the surgery more effectively. The goal is to make this technique more successful and widely usable by more surgeons. Participants in this study will undergo segmental resection surgery with the aid of advanced technology. The study uses 3D VR models to plan the surgery, providing a clearer view of the lung's anatomy before and during the operation. Additionally, a special imaging technique using a substance called Indocyanine Green (ICG) is used to help map out the lung segments more accurately during surgery. This trial is in its early stages, known as Phase I, and aims to assess how safe and feasible this approach is and how quickly surgeons can learn to use this new technology. The study does not outline specific risks or benefits but focuses on improving the precision and success rate of lung surgeries.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.89 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
Active ComparatorStudy Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
St. Joseph's Healthcare Hamilton
Hamilton, CanadaOpen St. Joseph's Healthcare Hamilton in Google Maps