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HepaRAS TRIAL: CHANGES IN HEPATECTOMY RISK ASSESSMENT WHEN INCORPORATING MEBROFENIN HIDA (HepaRAS)

Primary Purpose

Liver Failure as A Complication of Care, 30-day Mortality

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
mHBS
CT/MRI volumetry
Sponsored by
Nova Scotia Health Authority
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Liver Failure as A Complication of Care

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Future Liver Remnant Function (FLRF)

    Future Liver Remnant Volume (FLRV)

    Arm Description

    Preoperative FLRF risk assessment via 99mTc-mebrofenin hepatobiliary scintigraphy (mHBS)

    Preoperative FLRV assessment by CT/MRI volumetry

    Outcomes

    Primary Outcome Measures

    Post-hepatectomy liver failure (PHLF)
    Post-hepatectomy liver failure (PHLF)

    Secondary Outcome Measures

    The 50-50 criteria
    Prothrombin time <50% of normal and serum bilirubin >50 µmol/L on POD 5, which is an early predictor of more than 50% mortality rate after hepatectomy.
    Postoperative complications as per Clavien-Dindo classification
    Postoperative complications as per Clavien-Dindo classification
    Hospital length of stay
    Hospital length of stay
    30-day mortality
    30-day mortality

    Full Information

    First Posted
    March 6, 2022
    Last Updated
    March 14, 2022
    Sponsor
    Nova Scotia Health Authority
    Collaborators
    McGill University Health Centre/Research Institute of the McGill University Health Centre
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05280990
    Brief Title
    HepaRAS TRIAL: CHANGES IN HEPATECTOMY RISK ASSESSMENT WHEN INCORPORATING MEBROFENIN HIDA
    Acronym
    HepaRAS
    Official Title
    HepaRAS TRIAL: CHANGES IN HEPATECTOMY RISK ASSESSMENT WHEN INCORPORATING MEBROFENIN HIDA FOR FUNCTIONAL EVALUATION OF THE LIVER REMNANT: A PILOT STUDY
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    April 15, 2022 (Anticipated)
    Primary Completion Date
    May 30, 2024 (Anticipated)
    Study Completion Date
    August 30, 2025 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Nova Scotia Health Authority
    Collaborators
    McGill University Health Centre/Research Institute of the McGill University Health Centre

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Surgical procedures to remove a significant portion of the liver are used to treat various diseases including cancer. They have demonstrated to be the most effective treatment for selected patients. These procedures rely on the fascinating ability of the liver to grow back, allowing surgeons to remove of up to 70% of the organ in a safe manner. However, there are instances where severe complications and death occur due to the inability of the residual liver to perform all functions. It is estimated that up to 32% of patients undergoing this type of surgery will experience such complications. To prevent this, physicians calculate the total liver volume before surgery using radiology and estimate how much liver will remain after surgery. Only when the liver remnant is 30% or higher, the procedure is deemed safe. One of the main limitations of this strategy is that the estimated percentage of the liver remnant does not entirely reflect a proportional function. To overcome this limitation and avoid serious complications, a more precise assessment is required. Recently, a new scan was introduced using mebrofenin, which is metabolized in the liver and can be traced in a particular region of the organ using computer software. As a result, we can know with certainty, the percentual function of a portion of the liver, and if that portion will be sufficient to avoid complications and death after a major liver operation. This project proposes incorporating this technology for preoperative evaluation against our traditional assessment using just volume calculations. Participants will be randomly assigned to the traditional volume calculation or the new scan with mebrofenin, and we will compare how well both methods are able to predict complications and death after surgery. We are particularly interested in demonstrating if major complications and death after surgery are less using the new mebrofenin scan. Our study evaluating the introduction of a new and relatively harmful technique will help to better identify those patients with high risk for complications and death after a major surgical procedure on the liver. This will help in better selecting future patients and will allow for a more precise discussion during initial evaluation.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Liver Failure as A Complication of Care, 30-day Mortality

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    Hypothesis: Using Future Liver Remnant Function (FLRF) through 99mTc-mebrofenin hepatobiliary scintigraphy (mHBS) to select patients for major hepatectomy will reduce the rate of Post-hepatectomy liver failure (PHLF), compared to our standard-of-care Future Liver Remnant Volume (FLRV) calculations for patient selection. Methods: This is a prospective pilot study designed to evaluate feasibility and safety in the Canadian settings and will include patients undergoing major liver resection at the Queen Elizabeth II Health Sciences Centre (QEII) in Halifax, Canada, and at McGill University Health Centre in Montreal, Canada (McGill). Recruited patients, irrespective of their underlying liver quality will be randomly assigned via block randomization to have either preoperative FLRV assessment by CT/MRI volumetry or preoperative FLRF risk assessment via mHBS.
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    60 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Future Liver Remnant Function (FLRF)
    Arm Type
    Experimental
    Arm Description
    Preoperative FLRF risk assessment via 99mTc-mebrofenin hepatobiliary scintigraphy (mHBS)
    Arm Title
    Future Liver Remnant Volume (FLRV)
    Arm Type
    Active Comparator
    Arm Description
    Preoperative FLRV assessment by CT/MRI volumetry
    Intervention Type
    Diagnostic Test
    Intervention Name(s)
    mHBS
    Intervention Description
    Preoperative FLRF assessment using 99mTc-mebrofenin hepatobiliary scintigraphy (mHBS).
    Intervention Type
    Diagnostic Test
    Intervention Name(s)
    CT/MRI volumetry
    Intervention Description
    Preoperative FLRF assessment using CT/MRI volumetry
    Primary Outcome Measure Information:
    Title
    Post-hepatectomy liver failure (PHLF)
    Description
    Post-hepatectomy liver failure (PHLF)
    Time Frame
    30 days
    Secondary Outcome Measure Information:
    Title
    The 50-50 criteria
    Description
    Prothrombin time <50% of normal and serum bilirubin >50 µmol/L on POD 5, which is an early predictor of more than 50% mortality rate after hepatectomy.
    Time Frame
    5 days
    Title
    Postoperative complications as per Clavien-Dindo classification
    Description
    Postoperative complications as per Clavien-Dindo classification
    Time Frame
    30 days
    Title
    Hospital length of stay
    Description
    Hospital length of stay
    Time Frame
    30 days
    Title
    30-day mortality
    Description
    30-day mortality
    Time Frame
    30 days

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    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.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Boris Gala-Lopez
    Phone
    1 (902) 473 - 7411
    Email
    b.gala-lopez@dal.ca
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Boris Gala-Lopez, MD, MSC, PhD
    Organizational Affiliation
    Queen Elizabeth II Health Sciences Centre. Dalhousie University
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    PubMed Identifier
    22441614
    Citation
    Guglielmi A, Ruzzenente A, Conci S, Valdegamberi A, Iacono C. How much remnant is enough in liver resection? Dig Surg. 2012;29(1):6-17. doi: 10.1159/000335713. Epub 2012 Mar 15.
    Results Reference
    background
    PubMed Identifier
    30386047
    Citation
    Gupta M, Choudhury PS, Singh S, Hazarika D. Liver Functional Volumetry by Tc-99m Mebrofenin Hepatobiliary Scintigraphy before Major Liver Resection: A Game Changer. Indian J Nucl Med. 2018 Oct-Dec;33(4):277-283. doi: 10.4103/ijnm.IJNM_72_18.
    Results Reference
    background
    PubMed Identifier
    19937195
    Citation
    de Graaf W, van Lienden KP, Dinant S, Roelofs JJ, Busch OR, Gouma DJ, Bennink RJ, van Gulik TM. Assessment of future remnant liver function using hepatobiliary scintigraphy in patients undergoing major liver resection. J Gastrointest Surg. 2010 Feb;14(2):369-78. doi: 10.1007/s11605-009-1085-2.
    Results Reference
    background
    PubMed Identifier
    15181131
    Citation
    Bennink RJ, Dinant S, Erdogan D, Heijnen BH, Straatsburg IH, van Vliet AK, van Gulik TM. Preoperative assessment of postoperative remnant liver function using hepatobiliary scintigraphy. J Nucl Med. 2004 Jun;45(6):965-71.
    Results Reference
    background

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    HepaRAS TRIAL: CHANGES IN HEPATECTOMY RISK ASSESSMENT WHEN INCORPORATING MEBROFENIN HIDA

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