Feasibility and Utility of Artificial Intelligence (AI) / Machine Learning (ML) - Driven Advanced Intraoperative Visualization and Identification of Critical Anatomic Structures and Procedural Phases in Laparoscopic Cholecystectomy
Cholecystitis, Cholelithiasis, Biliary Dyskinesia
About this trial
This is an interventional diagnostic trial for Cholecystitis focused on measuring artificial intelligence, laparoscopy, laparoscopic surgery
Eligibility Criteria
Inclusion Criteria All patients age > 18 years old who are planned for elective laparoscopic cholecystectomy; spoken command and literacy in the native language spoken at each participating center; ability to understand and follow study procedures; and having provided signed consent. Eligible patients will be screened and assigned as per risk calculator for difficulty of LC Diagnosis: All patients with clinical suspicion and diagnosis of symptomatic cholelithiasis or cholecystitis planned for cholecystectomy. Typical imaging as per standard workup findings including US, CT and/or MRI. Plain radiographs and contrast imaging may be obtained by referring physicians and are helpful for confirming the clinical diagnosis. Prior therapy: o Patients with prior surgery are eligible for enrollment. Laboratory: Hemoglobin > 9 g/dL Platelet count ≥75,000/µL (may receive transfusions) Normal prothrombin time (PT), partial thromboplastin time (PTT) and international normalized ratio (INR) < 1.5 x upper limit of normal (including patients on prophylactic anticoagulation) Liver Function Test Renal function: Age-adjusted normal serum creatinine Adequate pulmonary function: Defined as no dyspnea at rest, and a pulse oximetry >94% on room air if there is any clinical indication for determination. Exclusion Criteria Non-elective acute cholecystectomy will be excluded. Patients assigned to FDA cleared ICG-based visualization are contraindicated for any chronic renal dysfunction, potential drug interaction, history of allergy to ICG or anaphylaxis, and pregnancy. Patients eligible for cholecystectomy, exclusion criteria include known allergy to ICG; coagulopathy or known, pre-existing liver disease; pregnancy or breast-feeding; or being of reproductive age with pregnancy possible and not ruled out. Patients currently in any investigational agents. Adults unable to consent Individuals under 18 years of age Pregnant women Prisoners Vulnerable populations
Sites / Locations
- Memorial Hermann Texas Medical Center
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Indocyanine green (ICG)
Non-Indocyanine Green (Non-ICG)
Patients in this arm will receive an intravenous injection of indocyanine green (ICG) 45 minutes prior to the start of surgery. This will be used to visualize the biliary anatomy using ActivSight, a device that is FDA 510(k)-cleared for this indication. The surgeon will perform the procedure in their standard fashion using ActivSight. ActivInsight artificial intelligence will be used to analyze the surgical video in real time to identify anatomic structures and phases of surgery.
The surgeon will perform the procedure in their standard fashion without the use of ICG. ActivInsight artificial intelligence will be used to analyze the surgical video in real time to identify anatomic structures and phases of surgery.