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Warfarin Prevents Portal Vein Thrombosis in Liver Cirrhotic Patients With Hypersplenism After Laparoscopic Splenectomy (ESWA)

Primary Purpose

Cirrhosis, Hypertension, Venous Thrombosis

Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Warfarin
Dipyridamole
Aspirin
Low Molecular Weight Heparin
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 Warfarin, Portal Vein, Anticoagulants, Cirrhosis, Hypertension, Venous Thrombosis, Splenectomy

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, Platelet count < 50*10^9/L
  • No evidence of PVT or spleno-mesenteric thrombosis by ultrasound evaluation and angio-CT
  • Informed consent to participate in the study

Exclusion Criteria:

  • Hepatocellular carcinoma or any other malignancy
  • Hypercoagulable state other than the liver disease related
  • DRUGS- oral contraceptives, anticoagulation or anti-platelet drugs
  • Base line INR >2
  • Child-Pugh grade C
  • Recent peptic ulcer disease
  • History of Hemorrhagic stroke
  • Pregnancy
  • Uncontrolled Hypertension
  • Age>75 yrs
  • F2 varices with red whale marks or F3 varices
  • Bleeding portal hypertension
  • Human immunodeficiency virus (HIV) infection

Sites / Locations

  • Clinical Medical College of Yangzhou UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Warfarin with dipyridamole

Aspirin with dipyridamole

Arm Description

From postoperative day 3, patients will receive dipyridamole 25mg tid for three months along with subcutaneous Low Molecular Weight Heparin Calcium injection for first five days and Warfarin 2.5mg qd with titration of dose to maintain a target INR of 2-3. Intially the INR will be monitored twice weekly with gradual escalation of dose to achieve target INR. After achieving the target INR, this is to be repeated every 4 weeks. The Doppler Ultra Sonography screening will be done every 3 months to assess the occurrence of portal vein thrombus, but the medications will be continue for one year irrespective of the occurrence of portal vein thrombus.

From postoperative day 3, patients will receive oral dipyridamole 25mg tid for three months along with subcutaneous injection of Low Molecular Weight Heparin (4100 IU) for first five days and Aspirin Enterie Ccoated Tablets 100mg qd for one year.

Outcomes

Primary Outcome Measures

Proportions of patients who will suffer from PVT or spleno-mesenteric thrombosis between oral anticoagulant Warfarin with dipyridamole group and oral Aspirin with dipyridamole group during the study period of 3 year from randomization

Secondary Outcome Measures

Proportions of patients who will show improvement in Child Pugh (>2 points)in both groups
Proportions of patients who will show improvement in Model for End Stage Liver Disease (MELD)(>4 points)in both groups
Proportions of patients who will show decrease in hepatic decompensation defined as development of ascites, PSE, portal hypertensive bleeding, jaundice, spontaneous bacterial peritonitis, or systemic infection
Proportions of patients who will suffer from hepatocellular carcinoma
Overall survival in both groups

Full Information

First Posted
September 4, 2014
Last Updated
December 30, 2018
Sponsor
Yangzhou University
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1. Study Identification

Unique Protocol Identification Number
NCT02238444
Brief Title
Warfarin Prevents Portal Vein Thrombosis in Liver Cirrhotic Patients With Hypersplenism After Laparoscopic Splenectomy
Acronym
ESWA
Official Title
Efficacy and Safety of Warfarin Anticoagulation for Prevention of Portal Vein Thrombosis in Liver Cirrhotic Patients With Hypersplenism After Laparoscopic Splenectomy
Study Type
Interventional

2. Study Status

Record Verification Date
December 2018
Overall Recruitment Status
Unknown status
Study Start Date
September 1, 2014 (undefined)
Primary Completion Date
September 30, 2019 (Anticipated)
Study Completion Date
September 30, 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Yangzhou University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine whether Warfarin Anticoagulation are effective and safe in Prevention of Portal Vein Thrombosis in Liver Cirrhotic Patients with Hypersplenism after Laparoscopic Splenectomy.
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 Doppler parameter will be recorded and the patient will be randomized into either interventional (warfarin) or control (aspirin) group. From postoperative day 3, patients in interventional (warfarin) group will receive oral Warfarin 2.5mg qd with titration of dose to maintain a target INR of 2-3 for 1 year, patients in control (aspirin) group will receive oral Aspirin Enterie Ccoated Tablets 100mg qd for 1 year, and both groups will be along with five days of subcutaneous injection of Low Molecular Weight Heparin and three months of oral Dipyridamole. Every 3 months the Doppler screening for the occurrence of portal vein thrombus (PVT) or spleno-mesenteric thrombosis will be done for all patients. Both groups will receive the therapy for one year irrespective of the Doppler findings in relation to portal vein thrombus occurrence. 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, Venous Thrombosis, Status; Splenectomy
Keywords
Warfarin, Portal Vein, Anticoagulants, Cirrhosis, Hypertension, Venous Thrombosis, Splenectomy

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Warfarin with dipyridamole
Arm Type
Experimental
Arm Description
From postoperative day 3, patients will receive dipyridamole 25mg tid for three months along with subcutaneous Low Molecular Weight Heparin Calcium injection for first five days and Warfarin 2.5mg qd with titration of dose to maintain a target INR of 2-3. Intially the INR will be monitored twice weekly with gradual escalation of dose to achieve target INR. After achieving the target INR, this is to be repeated every 4 weeks. The Doppler Ultra Sonography screening will be done every 3 months to assess the occurrence of portal vein thrombus, but the medications will be continue for one year irrespective of the occurrence of portal vein thrombus.
Arm Title
Aspirin with dipyridamole
Arm Type
Active Comparator
Arm Description
From postoperative day 3, patients will receive oral dipyridamole 25mg tid for three months along with subcutaneous injection of Low Molecular Weight Heparin (4100 IU) for first five days and Aspirin Enterie Ccoated Tablets 100mg qd for one year.
Intervention Type
Drug
Intervention Name(s)
Warfarin
Other Intervention Name(s)
Warfarin Sodium, Athrombine, COUMADIN, PANAWARFIN
Intervention Description
From postoperative day 3, patients will receive oral Warfarin 2.5mg qd with titration of dose to maintain a target INR of 2-3 for 1 year.
Intervention Type
Drug
Intervention Name(s)
Dipyridamole
Other Intervention Name(s)
Gardoxin, Coribon, Curantyl, Dilaplus
Intervention Description
From postoperative day 3, patients will receive oral dipyridamole 25mg tid for three months.
Intervention Type
Drug
Intervention Name(s)
Aspirin
Other Intervention Name(s)
Acenterine, Acetard, Acetophen
Intervention Description
From postoperative day 3, patients will receive oral Aspirin Enterie Ccoated Tablets 100mg qd for 1 year.
Intervention Type
Drug
Intervention Name(s)
Low Molecular Weight Heparin
Other Intervention Name(s)
Fraxiparine
Intervention Description
From postoperative day 3, Patients will receive subcutaneous injection of Low Molecular Weight Heparin (4100 IU) once daily for first five days.
Primary Outcome Measure Information:
Title
Proportions of patients who will suffer from PVT or spleno-mesenteric thrombosis between oral anticoagulant Warfarin with dipyridamole group and oral Aspirin with dipyridamole group during the study period of 3 year from randomization
Time Frame
3 years
Secondary Outcome Measure Information:
Title
Proportions of patients who will show improvement in Child Pugh (>2 points)in both groups
Time Frame
3 years
Title
Proportions of patients who will show improvement in Model for End Stage Liver Disease (MELD)(>4 points)in both groups
Time Frame
3 years
Title
Proportions of patients who will show decrease in hepatic decompensation defined as development of ascites, PSE, portal hypertensive bleeding, jaundice, spontaneous bacterial peritonitis, or systemic infection
Time Frame
3 years
Title
Proportions of patients who will suffer from hepatocellular carcinoma
Time Frame
3 years
Title
Overall survival in both groups
Time Frame
3 years

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, Platelet count < 50*10^9/L No evidence of PVT or spleno-mesenteric thrombosis by ultrasound evaluation and angio-CT Informed consent to participate in the study Exclusion Criteria: Hepatocellular carcinoma or any other malignancy Hypercoagulable state other than the liver disease related DRUGS- oral contraceptives, anticoagulation or anti-platelet drugs Base line INR >2 Child-Pugh grade C Recent peptic ulcer disease History of Hemorrhagic stroke Pregnancy Uncontrolled Hypertension Age>75 yrs F2 varices with red whale marks or F3 varices Bleeding portal hypertension Human immunodeficiency virus (HIV) infection
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Guo-Qing Jiang, MS
Phone
86-514-87373272
Email
jgqing2003@hotmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Dou-sheng Bai, MD
Phone
86-514-87373275
Email
bdsno1@hotmail.com
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, MS
Organizational Affiliation
Clinical Medical College of Yangzhou University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Ping Chen, MD
Organizational Affiliation
Clinical Medical College of Yangzhou University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Sheng-Jie Jin
Organizational Affiliation
Clinical Medical College of Yangzhou University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Clinical Medical College of Yangzhou University
City
Yangzhou
State/Province
Jiangsu
ZIP/Postal Code
225001
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Luo-Jing Zhou, MD
Phone
86-514-87373037
Email
luojing76@163.com
First Name & Middle Initial & Last Name & Degree
Dou-Sheng Bai, MD

12. IPD Sharing Statement

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Warfarin Prevents Portal Vein Thrombosis in Liver Cirrhotic Patients With Hypersplenism After Laparoscopic Splenectomy

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