Comparison of Icg's Route of Administration During Laparoscopic Cholecystectomy
Laparoscopic; Cholecystectomy, Cholelithiasis; Bile Duct, Choledocholithiasis
About this trial
This is an interventional prevention trial for Laparoscopic; Cholecystectomy
Eligibility Criteria
Inclusion Criteria:
- age older than 18 years old
- laparoscopic cholecystectomy
- elective surgery
Exclusion Criteria:
- younger than 18 years old
- no consent to participate to the study
- history of allergic reaction to iodine products
- urgent or emergent cholecystectomy
Sites / Locations
- General Hospital of Thessaloniki "G. Papanikolaou"Recruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Active Comparator
Active Comparator
Active Comparator
Group A (standard cholangiography during surgery)
Group B (cholangiography with iv administration of icg prior to surgery)
Group C (cholangiography with direct administration of icg to the bile duct system during surgery)
All patients will undergo laparoscopic cholecystectomy. In this group standard cholangiography will be performed during surgery. Standard cholangiography will be performed with selective catheterization of the cystic duct and infusion of a radiolucent substance (non-ionic low osmotic iodine). The category includes drugs such as iohexol, iopamidol, iopromide, ioversol, iobitriol, iomeprol and iodixanol. In our study we will use Xenetix (iobitriol) and perform cholangiography with C-ARM recording.
All patients will undergo laparoscopic cholecystectomy. In this group intravenous fluorescent cholangiography with indocyanine green will be given at a dose of 0.3 mg / mL / Kg 6 (six) hours before the start of surgery.The bile duct system will be recorded with a special camera (Karl Storz NIR / ICG).
All patients will undergo laparoscopic cholecystectomy. In the third group intraoperative cholangiography will be performed with direct administration of indocyanine green at a dose of 0.03 mg / ml / Kg to the bile duct cyst.