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

Instituto de Investigación Biomédica de Salamanca

Status and phase: Not yet enrolling; Phase 4

Conditions: Laparoscopic Cholecystectomy Surgery

Treatments: Drug: Intravenous injection of indocianine green at least three hours before surgery at a dose of 2.5 mg per subject.; Drug: Intravenous injection of indocianine green 15 to 30 minutes before surgery at a dose of 0.25 mg per subject.

Study type: Interventional

Funder types: Other

Identifiers

NCT07195331

Low-DOTIG

2025-522535-33-00 (EU Trial (CTIS) Number)

Details and patient eligibility

About

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 León, 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.

Enrollment: 122 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age ≥18 years.
• Signed informed consent.
• Indication for laparoscopic cholecystectomy (symptomatic cholelithiasis or gallbladder polyps).

Exclusion criteria

• Age <18 years.
• Pregnancy or lactation.
• Chronic kidney disease (stage >IIIb).
• ICG allergy.
• Allergy to other iodinated contrast
• Functional thyroid disease.
• Emergency non-deferrable surgery.
• Open approach.
• Suspicion of gallbladder cancer.
• Inability to understand the study.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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122 participants in 2 patient groups

2.5 mg >3h before surgery

Experimental group

Treatment:

Drug: Intravenous injection of indocianine green at least three hours before surgery at a dose of 2.5 mg per subject.

0.25 mg 15-30 min before surgery

Experimental group

Treatment:

Drug: Intravenous injection of indocianine green 15 to 30 minutes before surgery at a dose of 0.25 mg per subject.