Comparison Between Standard and Reduced Doses of Indocyanine Green in Fluorescence Cholangiography During Laparoscopic Cholecystectomy.

• Status: NOT_YET_RECRUITING
• Trial end date: 2027-01-31

Summary

Introduction:

This protocol outlines a randomized phase IV clinical trial designed to compare the efficacy of two different doses of indocyanine green (ICG) used in near-infrared fluorescent cholangiography during laparoscopic cholecystectomy (LC)-the current gold standard treatment for symptomatic cholelithiasis. Despite its effectiveness, LC is still associated with significant risks, particularly bile duct injury (BDI), a severe complication that this study aims to mitigate.

Phase: Phase IV Study design: Multicenter, randomized, open-label, parallel-group clinical trial (modified intention-to-treat).

Objectives:

Primary objective:

• To analyze differences between treatment groups (standard dose 2.5 mg \>3h preoperative vs reduced dose 0.25 mg immediate preoperative 15-30 min) during laparoscopic cholecystectomy in:
• Visualization of extrahepatic biliary structures
• Degree of visualization
• Degree of background liver fluorescence interference
• Perceived utility of the technique

Secondary objectives:

• Influence of BMI, biliary pathology type, surgery type, prior inflammation, surgical difficulty, previous instrumentation, and laparoscopic imaging system on results
• Intraoperative and postoperative complication rates
• 30-day mortality
• Impact on operative time and hospital stay
• Correlation between subjective and objective fluorescence assessment (ducts-to-liver fluorescence ratio) Population: Patients 18 years indicated for laparoscopic cholecystectomy (elective, early or urgent deferred).

Main inclusion criteria:

• Age 18 years
• Signed informed consent
• Indication for laparoscopic cholecystectomy (symptomatic cholelithiasis, gallbladder polyps with surgical indication)

Main exclusion criteria:

• Age \<18 years
• Pregnancy or lactation
• Chronic kidney disease (stage \>IIIb)
• ICG or iodinated contrast allergy
• Functional thyroid disease
• Emergency non-deferrable surgery
• Open approach
• Suspicion of gallbladder carcinoma
• Inability to understand the study Investigational product: Indocyanine green (ICG), intravenous administration

This multicenter study involves two hospitals in Castilla y Len, Spain, and plans to enroll 122 adult patients meeting specific clinical criteria for LC. Participants will be randomized into two treatment arms and will receive ICG accordingly:

• Group 1: 2.5 mg \>3h before surgery
• Group 2: 0.25 mg 15-30 min before surgery Fluorescence will be assessed both subjectively by the surgical team and objectively through digital image analysis using specialized software to calculate the bile duct-to-liver fluorescence ratio (RFBH).

Endpoints:

• Rates and degree of biliary structure identification pre- and post-dissection
• Perceived utility of cholangiography
• Liver background fluorescence interference
• Ducts-to-liver fluorescence ratio Duration: 12 months recruitment + 1 month follow-up = total 13 months Countries: Spain Ethics: The study will be conducted in accordance with ICH-GCP, EU Clinical Trials Regulation No 536/2014, and applicable national regulations.

Beyond comparing the diagnostic performance of two dosing strategies, this study seeks to provide evidence supporting a more practical and logistically feasible approach for implementing ICG fluorescence cholangiography in routine surgical practice, without compromising diagnostic accuracy or patient safety.

• Phase: PHASE4

Details

• Lead Sponsor: Instituto de Investigacin Biomdica de Salamanca
• Collaborator: Spanish Association of Surgeons (AEC)