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Functional MRI-based Assessment of Terlipressin vs. Octreotide on Renal Function in Cirrhotic Patients With Acute Variceal Bleeding (CHESS1903)

Primary Purpose

Renal Function Disorder, Acute Variceal Bleeding

Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Terlipressin
Octreotide
Sponsored by
Nanfang Hospital, Southern Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Renal Function Disorder focused on measuring Functional MRI, Terlipressin, Octreotide, Renal function disorder, Acute variceal bleeding

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • clinically and/or pathologically diagnosed cirrhosis
  • with a clinical history of acute variceal bleeding (melena, hematemesis etc.) assessed as Child-Pugh class B or C
  • voluntarily participated in the study and able to provide written informed consent and able to understand and willing to comply with the requirements of the study

Exclusion Criteria:

  • pregnant or lactating woman
  • diagnosed or suspected malignancy (hepatocellular carcinoma, cholangiocarcinoma etc.)
  • with mental disease and unable to comply with MRI examination
  • with contraindications of terlipressin and octreotide
  • with other conditions judged inadequate for participation by the investigators.

Sites / Locations

  • The Second Affiliated Hospital of Anhui Medical University
  • The First Hospital of Lanzhou UniversityRecruiting
  • Guangdong Second Provincial General Hospital
  • Nanfang Hospital of Southern Medical University
  • Xingtai People's Hospital
  • Zhongda Hospital, Medical School, Southeast University
  • The Third Hospital of Zhenjiang Affiliated Jiangsu University
  • The Sixth People's Hospital of Shenyang
  • The Second Affiliated Hospital of Baotou Medical University
  • Tianjin Second People's Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Experimental group

Control group

Arm Description

Drug: Terlipressin. Terlipressin should be administrated with an initial dose of 1-2 mg intravenously and slowly injected (over 1 minute) while monitoring the heart rate and blood pressure. The maintenance dose should be administrated every 4-6 hours. Each dose of terlipressin is 1mg. The usual duration of therapy is 3-5 days.

Drug: Octreotide. Octreotide should be continuously and intravenously dripped at the speed of 0.025-0.05 mg/h and could be diluted with saline with the maximum duration of 5 days. The usual duration of therapy is 3-5 days.

Outcomes

Primary Outcome Measures

Renal function
Number of participants with the improvement of renal function assessed by serum creatinine

Secondary Outcome Measures

Renal perfusion
Number of participants with the improvement of renal perfusion assessed by functional MRI measurement (intravoxel incoherent motion)
Renal blood oxygenation
Number of participants with the improvement of renal blood oxygenation assessed by functional MRI measurement (blood oxygen level dependent)
Failure to control bleeding
The occurrence rate of failure to control bleeding
Intra-hospital rebleeding
The occurrence rate of intra-hospital rebleeding
Intra-hospital mortality
The occurrence rate of intra-hospital mortality
Adverse events
The occurrence rate of adverse events
Overall survival
The number of participants still alive with the 90 days follow-up

Full Information

First Posted
July 17, 2019
Last Updated
August 16, 2021
Sponsor
Nanfang Hospital, Southern Medical University
Collaborators
LanZhou University, Zhongda Hospital, Guangdong Second Provincial General Hospital, Xingtai People's Hospital, The Third Hospital of Zhenjiang Affiliated Jiangsu University, Tianjin Second People's Hospital, The Second Hospital of Anhui Medical University, The Sixth People's Hospital of Shenyang, The Second Affiliated Hospital of Baotou Medical College
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1. Study Identification

Unique Protocol Identification Number
NCT04028323
Brief Title
Functional MRI-based Assessment of Terlipressin vs. Octreotide on Renal Function in Cirrhotic Patients With Acute Variceal Bleeding (CHESS1903)
Official Title
Functional MRI-based Assessment of Terlipressin vs. Octreotide on Renal Function in Cirrhotic Patients With Acute Variceal Bleeding (CHESS1903): A Multicenter, Single-blind, Randomised Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2021
Overall Recruitment Status
Unknown status
Study Start Date
July 16, 2019 (Actual)
Primary Completion Date
July 15, 2020 (Actual)
Study Completion Date
October 15, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Nanfang Hospital, Southern Medical University
Collaborators
LanZhou University, Zhongda Hospital, Guangdong Second Provincial General Hospital, Xingtai People's Hospital, The Third Hospital of Zhenjiang Affiliated Jiangsu University, Tianjin Second People's Hospital, The Second Hospital of Anhui Medical University, The Sixth People's Hospital of Shenyang, The Second Affiliated Hospital of Baotou Medical College

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
Acute variceal bleeding is one of the critical complications in patients with cirrhosis. Due to remarkable improvements in diagnostic and therapeutic modalities such as vasoactive agents, endoscopic therapy and antibiotics, the overall prognosis has been improved during the past several decades. However, it is still associated with increased mortality that is still around 20% at 6 weeks. Patients with advanced cirrhosis have an intense overactivity of the endogenous vasoactive systems characterized by arterial hypotension and low peripheral vascular resistance. Severe renal vasoconstriction in consequence of marked arterial vasodilatation in splanchnic circulation triggers the reduction of glomerular filtration rate, and thus induces acute kidney injury (AKI)/hepatorenal syndrome (HRS), which have been further implicated in the increasing mortality in patients with cirrhosis. Renal functional magnetic resonance imaging (fMRI), a technique considered superior to the most common method used to estimate the glomerular filtration rate, allows for non-invasive, accurate measurements of renal structures and functions in both animals and humans. It has become increasingly prevalent in research and clinical applications. In recent years, renal fMRI has developed rapidly with progress in MRI hardware and emerging post-processing algorithms. Function related imaging markers could be acquired via renal fMRI, encompassing water molecular diffusion, perfusion, and oxygenation. The study will use phase contrast - MR angiography, intravoxel incoherent motion - diffusion weighted imaging (IVIM-DWI) and blood-oxgen-level-dependent (BOLD)-MRI to evaluate renal functional changes after using vasoactive medications in patients with cirrhosis. The rationale for the use of vasoactive medications, including terlipressin and octreotide, is to produce splanchnic vasoconstriction and reduce portal blood flow and portal pressure, thereby underpinning the application of these vasoactive drugs in the management of cirrhotic patients with acute variceal bleeding. Meanwhile, terlipressin has been recommended as the international first-line pharmacological therapy for the treatment of HRS because terlipressin may improve renal hemodynamics, improve renal function and potentially enable HRS a reversible condition without the need of liver transplantation. However, the renal protection effect of terlipressin vs. octreotide remains unknown. In this study, the investigators aim to conduct a multicenter, single-blind randomized controlled trial to compare the renal protection effect of terlipressin vs. octreotide assessed by fMRI in the management of cirrhotic patients with acute variceal bleeding.
Detailed Description
Gastroesophageal varices, the most relevant portal-system collaterals, and acute variceal bleeding are critical complications that result directly from portal hypertension in patients with cirrhosis. Gastroesophageal varices are present approximately in 50% of patients with cirrhosis. Their presence correlates with the severity of liver disease. Only 40% of Child-Pugh A patients have varices whilst 85% of the occurrence rate in Child-Pugh C patients. Due to remarkable improvements in diagnostic and therapeutic modalities such as vasoactive agents, endoscopic therapy and antibiotics, the overall prognosis has been improved during the past several decades. However, it is still associated with increased mortality, which is still around 20% at 6 weeks. Acute variceal bleeding is also responsible for a variety of other complications in patients with cirrhosis including acute on chronic liver failure, hepatorenal syndrome, ascites liquid infection and hepatic encephalopathy. Therefore, timely and effective control of acute variceal bleeding is of crucial importance for the prognosis in patients with cirrhosis. In the early stages of cirrhosis, when portal hypertension is moderate, increased cardiac output compensated for a modest reduction in the systemic vascular resistance, ensuring the arterial pressure and effective arterial blood volume to maintain within the normal limits. Patients with advanced cirrhosis have an intense overactivity of the endogenous vasoactive systems characterized by arterial hypotension and low peripheral vascular resistance. This cascade of events sets the stage for further renal vasoconstriction and renal sodium retention as the splanchnic and systemic vasodilatation worsens with the progression of cirrhosis. Severe renal vasoconstriction in consequence of marked arterial vasodilatation in splanchnic circulation triggers the reduction of glomerular filtration rate, and thus induces acute kidney injury (AKI)/ hepato-renal syndrome (HRS) which may implicate in the increasing mortality in patients with cirrhosis. Renal functional magnetic resonance imaging (fMRI), a technique considered superior to the most common method used to estimate the glomerular filtration rate, allows for non-invasive, accurate measurements of renal structures and functions in both animals and humans. It has become increasingly prevalent in research and clinical applications. In recent years, renal fMRI has developed rapidly with progress in MRI hardware and emerging post-processing algorithms. Function related imaging markers could be acquired via renal fMRI, encompassing water molecular diffusion, perfusion, and oxygenation. The study will use phase contrast - MR angiography, intravoxel incoherent motion - diffusion weighted imaging (IVIM-DWI) and blood-oxgen-level-dependent (BOLD)-MRI to evaluate renal functional changes after using vasoactive medications in patients with cirrhosis. The rationale for the use of vasoactive medications, including terlipressin and octreotide, is to produce splanchnic vasoconstriction and reduce portal blood flow and portal pressure, thereby underpinning the application of these vasoactive drugs in the management of cirrhotic patients with acute variceal bleeding. Meanwhile, terlipressin has been recommended as the international first-line pharmacological therapy for the treatment of HRS because terlipressin may improve renal hemodynamics, improve renal function in patients and potentially enable HRS a reversible condition without the need of liver transplantation. However, the renal protection effect of terlipressin vs. octreotide remains unknown. In this study, the investigators aim to conduct a multicenter, single-blind randomized controlled trial to compare the renal protection effect of terlipressin vs. octreotide assessed by fMRI in the management of cirrhotic patients with acute variceal bleeding.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Renal Function Disorder, Acute Variceal Bleeding
Keywords
Functional MRI, Terlipressin, Octreotide, Renal function disorder, Acute variceal bleeding

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Experimental group
Arm Type
Experimental
Arm Description
Drug: Terlipressin. Terlipressin should be administrated with an initial dose of 1-2 mg intravenously and slowly injected (over 1 minute) while monitoring the heart rate and blood pressure. The maintenance dose should be administrated every 4-6 hours. Each dose of terlipressin is 1mg. The usual duration of therapy is 3-5 days.
Arm Title
Control group
Arm Type
Active Comparator
Arm Description
Drug: Octreotide. Octreotide should be continuously and intravenously dripped at the speed of 0.025-0.05 mg/h and could be diluted with saline with the maximum duration of 5 days. The usual duration of therapy is 3-5 days.
Intervention Type
Drug
Intervention Name(s)
Terlipressin
Intervention Description
Terlipressin should be administrated intravenously while monitoring heart rate and blood pressure daily.
Intervention Type
Drug
Intervention Name(s)
Octreotide
Intervention Description
Octreotide should be continuously intravenously administrated while monitoring heart rate and blood pressure daily.
Primary Outcome Measure Information:
Title
Renal function
Description
Number of participants with the improvement of renal function assessed by serum creatinine
Time Frame
6 days
Secondary Outcome Measure Information:
Title
Renal perfusion
Description
Number of participants with the improvement of renal perfusion assessed by functional MRI measurement (intravoxel incoherent motion)
Time Frame
6 days
Title
Renal blood oxygenation
Description
Number of participants with the improvement of renal blood oxygenation assessed by functional MRI measurement (blood oxygen level dependent)
Time Frame
6 days
Title
Failure to control bleeding
Description
The occurrence rate of failure to control bleeding
Time Frame
6 days
Title
Intra-hospital rebleeding
Description
The occurrence rate of intra-hospital rebleeding
Time Frame
6 days
Title
Intra-hospital mortality
Description
The occurrence rate of intra-hospital mortality
Time Frame
6 days
Title
Adverse events
Description
The occurrence rate of adverse events
Time Frame
6 days
Title
Overall survival
Description
The number of participants still alive with the 90 days follow-up
Time Frame
90 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: clinically and/or pathologically diagnosed cirrhosis with a clinical history of acute variceal bleeding (melena, hematemesis etc.) assessed as Child-Pugh class B or C voluntarily participated in the study and able to provide written informed consent and able to understand and willing to comply with the requirements of the study Exclusion Criteria: pregnant or lactating woman diagnosed or suspected malignancy (hepatocellular carcinoma, cholangiocarcinoma etc.) with mental disease and unable to comply with MRI examination with contraindications of terlipressin and octreotide with other conditions 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
Shenghong Ju, MD
Organizational Affiliation
Zhongda Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Xingshun Qi, MD
Organizational Affiliation
General Hospital of Shenyang Military Area
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Xiaolong Qi, MD
Organizational Affiliation
LanZhou University
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Second Affiliated Hospital of Anhui Medical University
City
Hefei
State/Province
Anhui
Country
China
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xiangpeng Hu, MD
First Name & Middle Initial & Last Name & Degree
Xiangpeng Hu, MD
Facility Name
The First Hospital of Lanzhou University
City
Lanzhou
State/Province
Gansu
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xiaorong Mao, MD
First Name & Middle Initial & Last Name & Degree
Xiaorong Mao, MD
Facility Name
Guangdong Second Provincial General Hospital
City
Guangzhou
State/Province
Guangdong
Country
China
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ming Xu, MD
First Name & Middle Initial & Last Name & Degree
Ming Xu, MD
Facility Name
Nanfang Hospital of Southern Medical University
City
Guangzhou
State/Province
Guangdong
Country
China
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jinjun Chen, MD
First Name & Middle Initial & Last Name & Degree
Jinjun Chen, MD
Facility Name
Xingtai People's Hospital
City
Xingtai
State/Province
Hebei
Country
China
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dengxiang Liu, MD
First Name & Middle Initial & Last Name & Degree
Dengxiang Liu, MD
Facility Name
Zhongda Hospital, Medical School, Southeast University
City
Nanjing
State/Province
Jiangsu
Country
China
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ruihua Shi, MD
First Name & Middle Initial & Last Name & Degree
Ruihua Shi, MD
Facility Name
The Third Hospital of Zhenjiang Affiliated Jiangsu University
City
Zhenjiang
State/Province
Jiangsu
Country
China
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shengqiang Zou, MD
First Name & Middle Initial & Last Name & Degree
Shengqiang Zou, MD
Facility Name
The Sixth People's Hospital of Shenyang
City
Shenyang
State/Province
Liaoning
Country
China
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yi Ma, MD
First Name & Middle Initial & Last Name & Degree
Yi Ma, MD
Facility Name
The Second Affiliated Hospital of Baotou Medical University
City
Baotou
State/Province
Neimenggu
Country
China
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Limei Ren, MD
First Name & Middle Initial & Last Name & Degree
Limei Ren, MD
Facility Name
Tianjin Second People's Hospital
City
Tianjin
State/Province
Tianjin
Country
China
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jia Li, MD
First Name & Middle Initial & Last Name & Degree
Jia Li, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
19776409
Citation
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Results Reference
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Citation
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Results Reference
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PubMed Identifier
22614754
Citation
Wong F. Recent advances in our understanding of hepatorenal syndrome. Nat Rev Gastroenterol Hepatol. 2012 May 22;9(7):382-91. doi: 10.1038/nrgastro.2012.96.
Results Reference
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Citation
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Functional MRI-based Assessment of Terlipressin vs. Octreotide on Renal Function in Cirrhotic Patients With Acute Variceal Bleeding (CHESS1903)

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