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

Sponsor
Nanfang Hospital of Southern Medical University (Other)
Overall Status
Recruiting
CT.gov ID
NCT03783065
Collaborator
Shunde Hospital, Southern Medical University (Other), Xingtai People's Hospital (Other), Beijing 302 Hospital (Other), LanZhou University (Other)
40
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2
45.8
10
0.2

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Drug: Propranolol
  • Procedure: Laparoscopic splenectomy and pericardial devascularization
  • Procedure: Endoscopic therapy
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
HVPG-guided Laparoscopic Versus Endoscopic Therapy for Variceal Rebleeding in Portal Hypertension: A Multicenter Randomized Controlled Trial (CHESS1803)
Actual Study Start Date :
Jan 2, 2019
Actual Primary Completion Date :
Oct 28, 2019
Anticipated Study Completion Date :
Oct 28, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Experimental group

Procedure: Laparoscopic splenectomy and pericardial devascularization Drug: Propranolol

Drug: Propranolol
Propranolol was administrated orally while keeping monitoring heart rate and blood pressure daily.

Procedure: Laparoscopic splenectomy and pericardial devascularization
Including splenectomy and pericardial devascularizaion under laparoscopy

Active Comparator: Control group

Procedure: Endoscopic therapy Drug: Propranolol

Drug: Propranolol
Propranolol was administrated orally while keeping monitoring heart rate and blood pressure daily.

Procedure: Endoscopic therapy
Either endoscopic variceal ligation (EVL) or cyanoacrylate injection was applied according to the condition of varices

Outcome Measures

Primary Outcome Measures

  1. Variceal rebleeding [1 year]

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

Secondary Outcome Measures

  1. Overall survival [1 year]

    The number of participants still alive 1 year after the therapy

  2. Hepatocellular carcinoma occurrence [1 year]

    The occurrence rate of hepatocellular carcinoma 1 year after the therapy

  3. Venous thrombosis [1 year]

    The occurrence rate of venous thrombosis upon each follow-up

  4. Quality of life score [1 year]

    The quality of life score measured using the 36-item Short Form Health Survey (SF-36) questionnaire upon each follow-up.

  5. Karnofsky score [1 year]

    The Karnofsky score categorized into low (score 10-40), intermediate (50-70), and high (80-100) upon each follow-up.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 The Fifth Medical Center of Chinese PLA General Hospital Beijing Beijing China
2 The First Hospital of Lanzhou University Lanzhou Gansu China
3 Shunde Hospital, Southern Medical University Shunde Guangdong China
4 Xingtai People's Hospital Xingtai Hebei China

Sponsors and Collaborators

  • Nanfang Hospital of Southern Medical University
  • Shunde Hospital, Southern Medical University
  • Xingtai People's Hospital
  • Beijing 302 Hospital
  • LanZhou University

Investigators

  • Principal Investigator: Weidong Wang, MD, Shunde Hospital, Southern Medical University
  • Principal Investigator: Changzeng Zuo, MD, Xingtai People's Hospital
  • Principal Investigator: Xun Li, MD, LanZhou University
  • Study Chair: Xiaolong Qi, MD, Nanfang Hospital of Southern Medical University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Xiaolong Qi, Director, Hepatic Hemodynamic Lab, Nanfang Hospital of Southern Medical University
ClinicalTrials.gov Identifier:
NCT03783065
Other Study ID Numbers:
  • CHESS1803
First Posted:
Dec 20, 2018
Last Update Posted:
Aug 17, 2021
Last Verified:
Aug 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Xiaolong Qi, Director, Hepatic Hemodynamic Lab, Nanfang Hospital of Southern Medical University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 17, 2021