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HVPG-guided Laparoscopic Versus Endoscopic Therapy for Variceal Rebleeding in Portal Hypertension: A Multicenter Randomized Controlled Trial (CHESS1803)

Primary Purpose

Portal Hypertension, Variceal Rebleeding

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Propranolol
Laparoscopic splenectomy and pericardial devascularization
Endoscopic therapy
Sponsored by
Nanfang Hospital, Southern Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Portal Hypertension focused on measuring Variceal Rebleeding, Hepatic venous pressure gradient, Laparoscopic Therapy, Endoscopic Therapy

Eligibility Criteria

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

Inclusion Criteria:

  • Clinically and/or pathologically diagnosed cirrhosis with portal hypertension
  • History of varicial bleeding without receiving endoscopic treatment
  • HVPG values between 16-20 mmHg
  • ECOG score ≤ 2 or KPS score ≥ 60 during screening
  • Voluntarily participated in the study and able to provide written informed consent, understand and willing to comply with the requirements of the study
  • Child-Pugh class A or B

Exclusion Criteria:

  • Pregnant or breastfeeding women
  • Prior known or suspected malignancy (hepatocellular carcinoma, cholangiocarcinoma etc.)
  • Limited coagulation situation (Quick< 50%, PTT> 50 sec, thrombocyte count <50000 / μl or disturbed thrombocyte function)
  • Massive ascites
  • Child-Pugh class C
  • Refuse or inadequate for HVPG measurement
  • Other situations whose existence judged inadequate for participation by the investigators

Sites / Locations

  • The Fifth Medical Center of Chinese PLA General Hospital
  • The First Hospital of Lanzhou University
  • Shunde Hospital, Southern Medical University
  • Xingtai People's HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Experimental group

Control group

Arm Description

Procedure: Laparoscopic splenectomy and pericardial devascularization Drug: Propranolol

Procedure: Endoscopic therapy Drug: Propranolol

Outcomes

Primary Outcome Measures

Variceal rebleeding
The occurrence rate of gastroesophageal varices rebleeding within 1-year follow-up

Secondary Outcome Measures

Overall survival
The number of participants still alive 1 year after the therapy
Hepatocellular carcinoma occurrence
The occurrence rate of hepatocellular carcinoma 1 year after the therapy
Venous thrombosis
The occurrence rate of venous thrombosis upon each follow-up
Quality of life score
The quality of life score measured using the 36-item Short Form Health Survey (SF-36) questionnaire upon each follow-up.
Karnofsky score
The Karnofsky score categorized into low (score 10-40), intermediate (50-70), and high (80-100) upon each follow-up.

Full Information

First Posted
December 19, 2018
Last Updated
August 16, 2021
Sponsor
Nanfang Hospital, Southern Medical University
Collaborators
Southern Medical University, China, Xingtai People's Hospital, Beijing 302 Hospital, LanZhou University
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1. Study Identification

Unique Protocol Identification Number
NCT03783065
Brief Title
HVPG-guided Laparoscopic Versus Endoscopic Therapy for Variceal Rebleeding in Portal Hypertension: A Multicenter Randomized Controlled Trial (CHESS1803)
Official Title
HVPG-guided Laparoscopic Versus Endoscopic Therapy for Variceal Rebleeding in Portal Hypertension: A Multicenter Randomized Controlled Trial (CHESS1803)
Study Type
Interventional

2. Study Status

Record Verification Date
August 2021
Overall Recruitment Status
Unknown status
Study Start Date
January 2, 2019 (Actual)
Primary Completion Date
October 28, 2019 (Actual)
Study Completion Date
October 28, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Nanfang Hospital, Southern Medical University
Collaborators
Southern Medical University, China, Xingtai People's Hospital, Beijing 302 Hospital, LanZhou 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
The development of portal hypertension is a vital event in the natural progression of cirrhosis and is associated with severe complications including gastroesophageal varices bleeding. Cirrhotic patients with hemorrhagic shock and/or liver failure caused by variceal bleeding face a mortality of 5-20%. Hepatic venous pressure gradient (HVPG) is the recommended golden standard for portal pressure assessment globally with favorable consistency and repeatability. Reducing the HVPG to levels of 12mmHg or below is associated with protection of variceal hemorrhage. An HVPG> 16mmHg indicates a higher risk of death and HVPG ≥ 20mmHg predicts failure to control bleeding, early rebleeding, and death during acute variceal hemorrhage. The management of portal hypertension has showed a trend of diversification with the development of medication, endoscopy, radiological intervention and liver transplantation. Although medication and endoscopic therapy have achieved preferable effects and are recommended as standard of care for the prevention of variceal rebleeding, patients with HVPG≥ 16mmHg still have a high risk of treatment failure and a high rate of rebleeding. Recent years, early TIPS is recommended as the first-line therapy for the prevention of rebleeding in cirrhotic patients with HVPG≥ 20mmHg. However, for those with HVPG values between 16 to 20mmHg, there is still lack of strong evidence to demonstrate the best practice for the management. With the rapid advancement of laparoscopic device and technique, the utility of laparoscopic splenectomy and pericardial devascularization showed less surgical trauma, bleeding and complications while retaining dependable effects compared to traditional open surgery, especially for portal hypertension with hypersplenism. In the study, the investigators aim to conduct a multicenter randomized controlled trial to compare the safety and effectiveness of HVPG-guided (16 to 20mmHg) laparoscopic versus endoscopic therapy for variceal rebleeding in patients with portal hypertension.
Detailed Description
The development of portal hypertension is a vital event in the natural progression of cirrhosis and is associated with severe complications including gastroesophageal varices bleeding. Cirrhotic patients with hemorrhagic shock and/or liver failure caused by variceal bleeding face a mortality of 5-20%. Hepatic venous pressure gradient (HVPG) is the recommended golden standard for portal pressure assessment globally with favorable consistency and repeatability. Reducing the HVPG to levels of 12mmHg or below is associated with protection of variceal hemorrhage. An HVPG> 16mmHg indicates a higher risk of death and HVPG ≥ 20mmHg predicts failure to control bleeding, early rebleeding, and death during acute variceal hemorrhage. The management of portal hypertension has showed a trend of diversification with the development of medication, endoscopy, radiological intervention and liver transplantation. Although medication and endoscopic therapy have achieved preferable effects and are recommended as standard of care for the prevention of variceal rebleeding, patients with HVPG≥ 16mmHg still have a high risk of treatment failure and a high rate of rebleeding. Recent years, early TIPS is recommended as the first-line therapy for the prevention of rebleeding in cirrhotic patients with HVPG≥ 20mmHg. However, for those with HVPG values between 16 to 20mmHg, there is still lack of strong evidence to demonstrate the best practice for the management. With the rapid advancement of laparoscopic device and technique, the utility of laparoscopic splenectomy and pericardial devascularization showed less surgical trauma, bleeding and complications while retaining dependable effects compared to traditional open surgery, especially for portal hypertension with hypersplenism. In the study, the investigators aim to conduct a multicenter (Shunde Hospital of Southern Medical University, Xingtai People's Hospital, The Fifth Medical Center of Chinese PLA General Hospital, The First Hospital of Lanzhou University) randomized controlled trial to compare the safety and effectiveness of HVPG-guided (16 to 20mmHg) laparoscopic versus endoscopic therapy for variceal rebleeding in patients with portal hypertension.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Portal Hypertension, Variceal Rebleeding
Keywords
Variceal Rebleeding, Hepatic venous pressure gradient, Laparoscopic Therapy, Endoscopic Therapy

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Experimental group
Arm Type
Experimental
Arm Description
Procedure: Laparoscopic splenectomy and pericardial devascularization Drug: Propranolol
Arm Title
Control group
Arm Type
Active Comparator
Arm Description
Procedure: Endoscopic therapy Drug: Propranolol
Intervention Type
Drug
Intervention Name(s)
Propranolol
Intervention Description
Propranolol was administrated orally while keeping monitoring heart rate and blood pressure daily.
Intervention Type
Procedure
Intervention Name(s)
Laparoscopic splenectomy and pericardial devascularization
Intervention Description
Including splenectomy and pericardial devascularizaion under laparoscopy
Intervention Type
Procedure
Intervention Name(s)
Endoscopic therapy
Intervention Description
Either endoscopic variceal ligation (EVL) or cyanoacrylate injection was applied according to the condition of varices
Primary Outcome Measure Information:
Title
Variceal rebleeding
Description
The occurrence rate of gastroesophageal varices rebleeding within 1-year follow-up
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Overall survival
Description
The number of participants still alive 1 year after the therapy
Time Frame
1 year
Title
Hepatocellular carcinoma occurrence
Description
The occurrence rate of hepatocellular carcinoma 1 year after the therapy
Time Frame
1 year
Title
Venous thrombosis
Description
The occurrence rate of venous thrombosis upon each follow-up
Time Frame
1 year
Title
Quality of life score
Description
The quality of life score measured using the 36-item Short Form Health Survey (SF-36) questionnaire upon each follow-up.
Time Frame
1 year
Title
Karnofsky score
Description
The Karnofsky score categorized into low (score 10-40), intermediate (50-70), and high (80-100) upon each follow-up.
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: Clinically and/or pathologically diagnosed cirrhosis with portal hypertension History of varicial bleeding without receiving endoscopic treatment HVPG values between 16-20 mmHg ECOG score ≤ 2 or KPS score ≥ 60 during screening Voluntarily participated in the study and able to provide written informed consent, understand and willing to comply with the requirements of the study Child-Pugh class A or B Exclusion Criteria: Pregnant or breastfeeding women Prior known or suspected malignancy (hepatocellular carcinoma, cholangiocarcinoma etc.) Limited coagulation situation (Quick< 50%, PTT> 50 sec, thrombocyte count <50000 / μl or disturbed thrombocyte function) Massive ascites Child-Pugh class C Refuse or inadequate for HVPG measurement Other situations whose existence judged inadequate for participation by the investigators
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xiaolong Qi, MD
Phone
86-18588602600
Email
qixiaolong@vip.163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Weidong Wang, MD
Organizational Affiliation
Southern Medical University, China
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Changzeng Zuo, MD
Organizational Affiliation
Xingtai People's Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Xun Li, MD
Organizational Affiliation
LanZhou University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Xiaolong Qi, MD
Organizational Affiliation
Nanfang Hospital, Southern Medical University
Official's Role
Study Chair
Facility Information:
Facility Name
The Fifth Medical Center of Chinese PLA General Hospital
City
Beijing
State/Province
Beijing
Country
China
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zhiwei Li, MD
First Name & Middle Initial & Last Name & Degree
Zhiwei Li, MD
Facility Name
The First Hospital of Lanzhou University
City
Lanzhou
State/Province
Gansu
Country
China
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xun Li, M.D.
First Name & Middle Initial & Last Name & Degree
Xun Li, M.D.
Facility Name
Shunde Hospital, Southern Medical University
City
Shunde
State/Province
Guangdong
Country
China
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Weidong Wang, MD
First Name & Middle Initial & Last Name & Degree
Weidong Wang, MD
Facility Name
Xingtai People's Hospital
City
Xingtai
State/Province
Hebei
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Changzeng Zuo, MD
First Name & Middle Initial & Last Name & Degree
Changzeng Zuo, MD
First Name & Middle Initial & Last Name & Degree
Jitao Wang, MD

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
IPD data including age, gender, height, weight, ethnic, past history (including time of bleeding), dignosis, co-morbidity, medication, labortory test results (including blood routine, blood ammonia, clotting time, liver function and renal function), ultrasonic results (including spleen diameter, portal vein diameter, portal vein velocity, splenic vein velocity, etc.), transient elastography results (including liver and spleen stiffness), esophagogastroduodenoscopy results, Child-pugh score, QOL and KPS scores and time of all outcome events will be shared upon publication of this study.
IPD Sharing Time Frame
The data will become available upon publication of this study for 2 years.
IPD Sharing Access Criteria
Access application is approved by principal investigators.
Citations:
PubMed Identifier
30215362
Citation
Qi X, Berzigotti A, Cardenas A, Sarin SK. Emerging non-invasive approaches for diagnosis and monitoring of portal hypertension. Lancet Gastroenterol Hepatol. 2018 Oct;3(10):708-719. doi: 10.1016/S2468-1253(18)30232-2.
Results Reference
background
PubMed Identifier
25177367
Citation
Cremers I, Ribeiro S. Management of variceal and nonvariceal upper gastrointestinal bleeding in patients with cirrhosis. Therap Adv Gastroenterol. 2014 Sep;7(5):206-16. doi: 10.1177/1756283X14538688.
Results Reference
background
PubMed Identifier
20200386
Citation
Garcia-Tsao G, Bosch J. Management of varices and variceal hemorrhage in cirrhosis. N Engl J Med. 2010 Mar 4;362(9):823-32. doi: 10.1056/NEJMra0901512. No abstract available. Erratum In: N Engl J Med. 2011 Feb 3;364(5):490. Dosage error in article text.
Results Reference
background
PubMed Identifier
27786365
Citation
Garcia-Tsao G, Abraldes JG, Berzigotti A, Bosch J. Portal hypertensive bleeding in cirrhosis: Risk stratification, diagnosis, and management: 2016 practice guidance by the American Association for the study of liver diseases. Hepatology. 2017 Jan;65(1):310-335. doi: 10.1002/hep.28906. Epub 2016 Dec 1. No abstract available. Erratum In: Hepatology. 2017 Jul;66(1):304.
Results Reference
background
PubMed Identifier
26047908
Citation
de Franchis R; Baveno VI Faculty. Expanding consensus in portal hypertension: Report of the Baveno VI Consensus Workshop: Stratifying risk and individualizing care for portal hypertension. J Hepatol. 2015 Sep;63(3):743-52. doi: 10.1016/j.jhep.2015.05.022. Epub 2015 Jun 3. No abstract available.
Results Reference
background
PubMed Identifier
19724251
Citation
Bosch J, Abraldes JG, Berzigotti A, Garcia-Pagan JC. The clinical use of HVPG measurements in chronic liver disease. Nat Rev Gastroenterol Hepatol. 2009 Oct;6(10):573-82. doi: 10.1038/nrgastro.2009.149. Epub 2009 Sep 1.
Results Reference
background
PubMed Identifier
25438286
Citation
Saad WE. Endovascular management of gastric varices. Clin Liver Dis. 2014 Nov;18(4):829-51. doi: 10.1016/j.cld.2014.07.005. Epub 2014 Oct 16.
Results Reference
background
PubMed Identifier
22366180
Citation
de Souza AR, La Mura V, Reverter E, Seijo S, Berzigotti A, Ashkenazi E, Garcia-Pagan JC, Abraldes JG, Bosch J. Patients whose first episode of bleeding occurs while taking a beta-blocker have high long-term risks of rebleeding and death. Clin Gastroenterol Hepatol. 2012 Jun;10(6):670-6; quiz e58. doi: 10.1016/j.cgh.2012.02.011. Epub 2012 Feb 22. Erratum In: Clin Gastroenterol Hepatol. 2014 Jun;12(6):1056.
Results Reference
background
PubMed Identifier
32580978
Citation
Shao R, Li Z, Wang J, Qi R, Liu Q, Zhang W, Mao X, Song X, Li L, Liu Y, Zhao X, Liu C, Li X, Zuo C, Wang W, Qi X. Hepatic venous pressure gradient-guided laparoscopic splenectomy and pericardial devascularisation versus endoscopic therapy for secondary prophylaxis for variceal rebleeding in portal hypertension (CHESS1803): study protocol of a multicenter randomised controlled trial in China. BMJ Open. 2020 Jun 23;10(6):e030960. doi: 10.1136/bmjopen-2019-030960.
Results Reference
derived

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HVPG-guided Laparoscopic Versus Endoscopic Therapy for Variceal Rebleeding in Portal Hypertension: A Multicenter Randomized Controlled Trial (CHESS1803)

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