HepaRAS TRIAL: CHANGES IN HEPATECTOMY RISK ASSESSMENT WHEN INCORPORATING MEBROFENIN HIDA (HepaRAS)
Liver Failure as A Complication of Care, 30-day Mortality
About this trial
This is an interventional prevention trial for Liver Failure as A Complication of Care
Eligibility Criteria
Inclusion Criteria:
All adult patients who are being considered for major hepatectomy at the QEII and McGill for malignant or benign disease. Both open and laparoscopic approaches will be accepted in the study. Patients with underlying liver cirrhosis or receiving additional ablation therapies will not be excluded.
Exclusion Criteria:
Patients will be excluded if younger than 18 years-old, pregnant, or if the hepatectomy is associated with another major non-liver procedure. Patients will also be excluded if they do not qualify for major hepatectomy following FLRF or FLRV assessment.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Future Liver Remnant Function (FLRF)
Future Liver Remnant Volume (FLRV)
Preoperative FLRF risk assessment via 99mTc-mebrofenin hepatobiliary scintigraphy (mHBS)
Preoperative FLRV assessment by CT/MRI volumetry