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
About this trial
This is an interventional prevention trial for Portal Hypertension focused on measuring Portal Hypertension, Liver resection, Somatostatin
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.
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
NCT ID
NCT04010669
First Posted
June 28, 2019
Last Updated
July 4, 2019
Sponsor
Laikο General Hospital, Athens
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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