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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
Yangzhou University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cirrhosis focused on measuring Vagus nerve, Delayed gastric emptying, Cirrhosis, Hypertension, laparoscopy

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

First Posted
January 4, 2018
Last Updated
January 18, 2020
Sponsor
Yangzhou University
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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

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Modified Vagus Nerve-preserving Laparoscopic Splenectomy and Azygoportal Disconnection

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