Modified Vagus Nerve-preserving Laparoscopic Splenectomy and Azygoportal Disconnection (ESVLSD)
Primary Purpose
Cirrhosis, Hypertension, Splenectomy
Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Vagus nerve-preserving group
Sponsored by

About this trial
This is an interventional prevention trial for Cirrhosis focused on measuring Vagus nerve, Delayed gastric emptying, Cirrhosis, Hypertension, laparoscopy
Eligibility Criteria
Inclusion Criteria:
- A clinical, radiological or histologic diagnosis of cirrhosis of any etiology
- Splenomegaly with secondary hypersplenism
- Bleeding portal hypertension
- No evidence of portal vein system thrombosis by ultrasound evaluation and angio-CT
- Informed consent to participate in the study
Exclusion Criteria:
- Delayed gastric emptying
- Diarrhea
- Hepatocellular carcinoma or any other malignancy,
- Hypercoagulable state other than the liver disease related
- DRUGS- oral contraceptives, anticoagulation or anti-platelet drugs.
- Child - Pugh C
- Recent peptic ulcer disease
- History of Hemorrhagic stroke
- Pregnancy.
- Uncontrolled Hypertension
- Age>75 yrs
- Human immunodeficiency virus (HIV) infection
Sites / Locations
- Clinical Medical College of Yangzhou University
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Vagus nerve-preserving group
Conventional group
Arm Description
Every patient of vagus nerve-preserving group will receive the modified vagus nerve-preserving laparoscopic azygoportal disconnection procedure.
Every patient of conventional group will receive the conventional laparoscopic azygoportal disconnection procedure.
Outcomes
Primary Outcome Measures
Delayed gastric emptying
Proportions of patients who will suffer from delayed gastric emptying in both groups.
Secondary Outcome Measures
Postoperative complications of the digestive system
Proportions of patients who will suffer from postoperative complications of the digestive system in both groups.
Body weight
Proportions of patients who will show improvement in body weight both groups.
Hepatic decompensation
Proportions of patients who will suffer from hepatic decompensation defined as development of ascites, PSE, portal hypertensive bleeding, jaundice, spontaneous bacterial peritonitis, or systemic infection.
Portal vein system thrombosis
Proportions of patients who will suffer from portal vein system thrombosis in both groups.
Hepatocellular carcinoma
Proportions of patients who will suffer from hepatocellular carcinoma in both groups.
Overall survival
Overall survival in both groups.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03396796
Brief Title
Modified Vagus Nerve-preserving Laparoscopic Splenectomy and Azygoportal Disconnection
Acronym
ESVLSD
Official Title
Modified Vagus Nerve-preserving Versus Conventional Laparoscopic Splenectomy and Azygoportal Disconnection
Study Type
Interventional
2. Study Status
Record Verification Date
January 2020
Overall Recruitment Status
Completed
Study Start Date
April 9, 2018 (Actual)
Primary Completion Date
December 31, 2019 (Actual)
Study Completion Date
December 31, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Yangzhou University
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
This study aimed to evaluate whether vagus nerve-preserving laparoscopic splenectomy and azygoportal disconnection is effective and safe, and to determine whether a reduction in the incidence of postoperative complications of the digestive system improves postoperative quality of life compared with conventional laparoscopic splenectomy and azygoportal disconnection.
Detailed Description
After successful screening the cases of cirrhosis of liver irrespective of the etiology who have non tumor portal vein thrombosis will be enrolled. The baseline parameter will be recorded and the patient will be randomized into either interventional (vagus nerve-preserving laparoscopic splenectomy and azygoportal disconnection) or control (conventional laparoscopic splenectomy and azygoportal disconnection) group. From postoperative day 3, all patients will receive 100 mg oral aspirin enteric-coated tablets (Bayer, Leverkusen, Germany) once daily for 1 year, low-molecular-weight heparin (CS Bio, Hebei, China) subcutaneously (4.100 IU/day) for 5 days, and 25 mg of oral dipyridamole (Henan Furen, Henan, China) thrice daily for 3 months. At months 3, 9, and 12 after operation, electron gastroscopy examination for delayed gastric emptying will be done for all patients. Postoperative complications of the digestive system (including diarrhea, epigastric fullness, bloating, nausea, and vomiting), liver and renal function, and body weight will be recorded at the seventh day, months 1, 3, 6, 9, and 12 after operation. Then one year monitoring will be done in the both groups as per the primary or secondary outcome.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cirrhosis, Hypertension, Splenectomy, Laparoscopy
Keywords
Vagus nerve, Delayed gastric emptying, Cirrhosis, Hypertension, laparoscopy
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Vagus nerve-preserving group
Arm Type
Experimental
Arm Description
Every patient of vagus nerve-preserving group will receive the modified vagus nerve-preserving laparoscopic azygoportal disconnection procedure.
Arm Title
Conventional group
Arm Type
No Intervention
Arm Description
Every patient of conventional group will receive the conventional laparoscopic azygoportal disconnection procedure.
Intervention Type
Procedure
Intervention Name(s)
Vagus nerve-preserving group
Intervention Description
The modified vagus nerve-preserving procedure was performed in the following order: (1) left gastroepiploic vein along greater curvature; (2) the posterior surface of stomach, including the posterior gastric veins; (3) the left lateral surface of the distal esophagus; (4) the left inferior phrenic veins; (5) the posterior surface of the distal esophagus;(6) the anterior surface of the distal esophagus; and (7) the right lateral surface of the distal esophagus. The hepatogastric ligament was conserved. the adherent junction between visceral peritoneum and the right crural diaphragm, and divided it into the lesser omental sac. The left gastric artery and vein and the posterior gastric veins were transected en bloc using a linear laparoscopic vascular stapler.
Primary Outcome Measure Information:
Title
Delayed gastric emptying
Description
Proportions of patients who will suffer from delayed gastric emptying in both groups.
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Postoperative complications of the digestive system
Description
Proportions of patients who will suffer from postoperative complications of the digestive system in both groups.
Time Frame
1 year
Title
Body weight
Description
Proportions of patients who will show improvement in body weight both groups.
Time Frame
1 year
Title
Hepatic decompensation
Description
Proportions of patients who will suffer from hepatic decompensation defined as development of ascites, PSE, portal hypertensive bleeding, jaundice, spontaneous bacterial peritonitis, or systemic infection.
Time Frame
1 year
Title
Portal vein system thrombosis
Description
Proportions of patients who will suffer from portal vein system thrombosis in both groups.
Time Frame
1 year
Title
Hepatocellular carcinoma
Description
Proportions of patients who will suffer from hepatocellular carcinoma in both groups.
Time Frame
1 year
Title
Overall survival
Description
Overall survival in both groups.
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
A clinical, radiological or histologic diagnosis of cirrhosis of any etiology
Splenomegaly with secondary hypersplenism
Bleeding portal hypertension
No evidence of portal vein system thrombosis by ultrasound evaluation and angio-CT
Informed consent to participate in the study
Exclusion Criteria:
Delayed gastric emptying
Diarrhea
Hepatocellular carcinoma or any other malignancy,
Hypercoagulable state other than the liver disease related
DRUGS- oral contraceptives, anticoagulation or anti-platelet drugs.
Child - Pugh C
Recent peptic ulcer disease
History of Hemorrhagic stroke
Pregnancy.
Uncontrolled Hypertension
Age>75 yrs
Human immunodeficiency virus (HIV) infection
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dou-Sheng Bai, MD
Organizational Affiliation
Clinical Medical College of Yangzhou University
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Guo-Qing Jiang, MD
Organizational Affiliation
Clinical Medical College of Yangzhou University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ping Chen, MD
Organizational Affiliation
Clinical Medical College of Yangzhou University
Official's Role
Study Director
Facility Information:
Facility Name
Clinical Medical College of Yangzhou University
City
Yangzhou
State/Province
Jiangsu
ZIP/Postal Code
225001
Country
China
12. IPD Sharing Statement
Learn more about this trial
Modified Vagus Nerve-preserving Laparoscopic Splenectomy and Azygoportal Disconnection
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