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The Role of Somatostatin in the Hemodynamics of the Hepatic Circulation in Patients Undergoing Liver Resection

Primary Purpose

Portal Hypertension

Status
Unknown status
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Somatostatin
Placebo
Sponsored by
Laikο General Hospital, Athens
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Portal Hypertension focused on measuring Portal Hypertension, Liver resection, Somatostatin

Eligibility Criteria

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

Inclusion Criteria:

  • Patients undergoing hepatectomy for any reason including primary malignant liver tumors (hepatocellular carcinomas, cholangiocellular carcinomas, etc), metastatic liver disease and symptomatic benign liver lesions (liver adenomas, focal nodular hyperplasia, hemangiomas, etc).
  • Adult patients (≥18 years old)
  • Patients whose indication for hepatectomy will be decided by a multidisciplinary team meeting.
  • Patients who eill agree to sign an informed consent

Exclusion Criteria:

  • Patients who do not meet the inclusion criteria and those
  • Patients undergoing synchronous hepatectomy-colectomy.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Placebo Comparator

    Arm Label

    Study group

    Control group

    Arm Description

    The study group includes participants who will receive somatostatin postoperatively (after liver resection).

    The control group includes participants who will receive placebo (a 24 hours infusion of 1000ml Normal Saline solution 0.9%) postoperatively (after liver resection).

    Outcomes

    Primary Outcome Measures

    The effect of somatostatin in the regulation of velocity of the hepatic circulation at patients who have undergone hepatectomy.
    The velocity of the portal vein, splenic vein, hepatic artery and hepatic veins will be measured sonographically
    The effect of somatostatin in the regulation of diameter of the vessels of the hepatic circulation at patients who have undergone hepatectomy.
    The diameter of the portal vein, splenic vein, hepatic artery and hepatic veins will be measured sonographically
    The effect of somatostatin in the regulation of blood flow of the hepatic circulation at patients who have undergone hepatectomy.
    The blood flow of the portal vein, splenic vein, hepatic artery and hepatic veins will be calculated using the following mathematic formula: Flow= velocity x cross section area (the cross section area of the vessel can be calculated using the following equation: CSA=πr2, with 'r' representing the vessel's radius).

    Secondary Outcome Measures

    Full Information

    First Posted
    June 28, 2019
    Last Updated
    July 4, 2019
    Sponsor
    Laikο General Hospital, Athens
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04010669
    Brief Title
    The Role of Somatostatin in the Hemodynamics of the Hepatic Circulation in Patients Undergoing Liver Resection
    Official Title
    The Effect of Somatostatin in the Regulation of Velocity and Blood Flow of the Hepatic Circulation in Patients Undergoing Liver Resection
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    July 2019
    Overall Recruitment Status
    Unknown status
    Study Start Date
    August 1, 2019 (Anticipated)
    Primary Completion Date
    March 31, 2020 (Anticipated)
    Study Completion Date
    July 31, 2020 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Laikο General Hospital, Athens

    4. Oversight

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

    5. Study Description

    Brief Summary
    The purpose of the present clinical trial is to study the effect of somatostatin in the regulation of velocity and blood flow of the hepatic circulation in patients undergoing liver resection. The patients will be randomized in two groups: the study group will receive somatostatin and the control group will receive the placebo. In both groups, patients will undergo hepatectomy and directly postoperatively they will receive either somatostatin or placebo, depending on their randomization. The primary endpoint will be the increase or decrease of the velocity and the flow of the hepatic circulation estimated by ultrasonography compared to the same parameters when measured preoperatively.
    Detailed Description
    The purpose of the present clinical trial is to study the effect of somatostatin in the regulation of blood flow of the portal circulation at patients who have undergone hepatectomy. The patients will be randomized in two groups, namely the group that will receive somatostatin (study group) and the group that will receive the placebo (control group). In both groups, patients will undergo liver resection and directly postoperatively they will receive either somatostatin (2 amps at 1000ml normal saline solution in continuous 24-hour infusion for 5 days) or a 24 hours infusion of 1000ml Normal Saline solution 0.9%. On the first, third, fifth and seventh postoperative day, the velocity and the diameter of the portal vein, splenic vein, hepatic artery and hepatic veins will be measured sonographically and the flow will be calculated using the following mathematic formula: Flow= velocity x cross section area (the cross section area of the vessel can be calculated using the following equation: cross section area=πr2, with 'r' representing the vessel's radius). Preoperatively On the day before the surgery (day -1),an ultrasound will be performed in order to measure the velocity and the diameter of the portal vein, splenic vein, hepatic artery and hepatic veins and the flow will be calculated using the following mathematic formula: Flow= velocity x cross section area, as stated above. The following data will also be recorded: platelets, bilirubin (total and direct), albumin, cholesterol, urea, International Normalized Ratio, sodium, Serum Glutamic Oxaloacetic Transaminase, Serum Glutamic Pyruvic Transaminase, Alkaline Phosphatase, gamma-Glutamyl Transferase and the Model for End-stage Liver Disease score of each patient will be calculated. Finally, our patients will undergo a Computer Tomography scan in order to measure their liver and spleen volumetry. On the day of the surgery On the day of the surgery (day 0), the following information will be recorded: the type of the surgical procedure, the duration (in minutes), the presence of ascites, the number of times and total duration of the a pringle maneuver and finally the percentage of the resection of the parenchyma will be calculated. A biopsy of healthy liver tissue will be sent for histological examination in order to determine the presence of fibrosis/cirrhosis and its stage. Postoperatively On the first, third and fifth postoperative day (day 1, 3, 5), the preoperative blood test and the ultrasound measurements will be repeated and the amount of fluid in the drain(s) and inside the abdomen (via ultrasound) will be recorded. Finally, the fluid will be sent for biochemical examination and culture. On the seventh postoperative day (day 7) all blood, fluid and ultrasound measurements will be repeated and also the liver and spleen volumetry via CT.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Portal Hypertension
    Keywords
    Portal Hypertension, Liver resection, Somatostatin

    7. Study Design

    Primary Purpose
    Prevention
    Study Phase
    Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    Participant
    Allocation
    Randomized
    Enrollment
    40 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Study group
    Arm Type
    Active Comparator
    Arm Description
    The study group includes participants who will receive somatostatin postoperatively (after liver resection).
    Arm Title
    Control group
    Arm Type
    Placebo Comparator
    Arm Description
    The control group includes participants who will receive placebo (a 24 hours infusion of 1000ml Normal Saline solution 0.9%) postoperatively (after liver resection).
    Intervention Type
    Drug
    Intervention Name(s)
    Somatostatin
    Intervention Description
    2 amp of somatostatin at 1000ml normal saline solution in continuous 24-hour infusion for 5 days
    Intervention Type
    Drug
    Intervention Name(s)
    Placebo
    Intervention Description
    24 hours infusion of 1000ml Normal Saline solution 0.9%
    Primary Outcome Measure Information:
    Title
    The effect of somatostatin in the regulation of velocity of the hepatic circulation at patients who have undergone hepatectomy.
    Description
    The velocity of the portal vein, splenic vein, hepatic artery and hepatic veins will be measured sonographically
    Time Frame
    7 days
    Title
    The effect of somatostatin in the regulation of diameter of the vessels of the hepatic circulation at patients who have undergone hepatectomy.
    Description
    The diameter of the portal vein, splenic vein, hepatic artery and hepatic veins will be measured sonographically
    Time Frame
    7 days
    Title
    The effect of somatostatin in the regulation of blood flow of the hepatic circulation at patients who have undergone hepatectomy.
    Description
    The blood flow of the portal vein, splenic vein, hepatic artery and hepatic veins will be calculated using the following mathematic formula: Flow= velocity x cross section area (the cross section area of the vessel can be calculated using the following equation: CSA=πr2, with 'r' representing the vessel's radius).
    Time Frame
    7 days

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients undergoing hepatectomy for any reason including primary malignant liver tumors (hepatocellular carcinomas, cholangiocellular carcinomas, etc), metastatic liver disease and symptomatic benign liver lesions (liver adenomas, focal nodular hyperplasia, hemangiomas, etc). Adult patients (≥18 years old) Patients whose indication for hepatectomy will be decided by a multidisciplinary team meeting. Patients who eill agree to sign an informed consent Exclusion Criteria: Patients who do not meet the inclusion criteria and those Patients undergoing synchronous hepatectomy-colectomy.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Evgenia C Kotsifa, MD
    Phone
    00306986640874
    Email
    eugeniakotsifa@yahoo.gr
    First Name & Middle Initial & Last Name or Official Title & Degree
    Georgios C Sotiropoulos, MD, PhD
    Phone
    00306948111291
    Email
    gsotirop@yahoo.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Georgios C Sotiropoulos, MD, PhD
    Organizational Affiliation
    Assistant Professor of Surgery, Laiko Hospital
    Official's Role
    Study Chair

    12. IPD Sharing Statement

    Learn more about this trial

    The Role of Somatostatin in the Hemodynamics of the Hepatic Circulation in Patients Undergoing Liver Resection

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