A Combined Model Based on Spleen Stiffness, Liver Stiffness and Platelets for Assessing Portal Hypertension in Compensated Cirrhosis (CHESS2202)

Sponsor
Hepatopancreatobiliary Surgery Institute of Gansu Province (Other)
Overall Status
Recruiting
CT.gov ID
NCT05251272
Collaborator
LanZhou University (Other), Shulan Hospital of Hangzhou (Other), The Third People's Hospital of Taiyuan (Other), QuFu People's Hospital (Other), The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School (Other)
300
5
12
60
5

Study Details

Study Description

Brief Summary

Portal hypertension contributed to the main complications of liver cirrhosis. Currently, hepatic venous pressure gradient (HVPG) was the reference standard for evaluating portal pressure in patients with cirrhosis. However, the practice of HVPG is limited to require the extensive experience and highly specialized centers. In recent years, non-invasive methods were proposed to predict the degree of cirrhotic portal hypertension. Of them, liver stiffness measured by transient elastography had shown good performance for predicting clinically significant portal hypertension. However, liver stiffness only has a good correlation with portal pressure in the early stage of portal hypertension (HVPG<10 mmHg), because liver fibrosis is the main cause of portal hypertension in this period. In the stage of clinically significant portal hypertension (CSPH) (HVPG≥10 mmHg), increased portal vein inflow due to splanchnic vasodilation and hyperdynamic circulation, spleen stiffness may have a better correlation with HVPG than that of liver stiffness. Several studies have explored the combination of liver stiffness, platelet count and spleen stiffness for varices screening. However, there are few studies to report the above parameters for assessing CSPH and unneeded HVPG avoiding.

Since the spleen was stiffer than the liver, the current vibration-controlled transient elastography examination is dedicated to the liver, rather than the spleen. Very recently, a novel spleen-dedicated stiffness measured by transient elastography was proposed. The prospective, multicenter study aims to add spleen stiffness as a supplementary parameter to establish new criteria for identify CSPH in patients with compensated cirrhosis, with a dedicated probe on transient elastography equipment to assess spleen stiffness and liver stiffness, and further develop a novel model based on spleen stiffness for predicting the liver decompensation in patients with compensated cirrhosis.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Hepatic venous pressure gradient

Detailed Description

Portal hypertension contributed to the main complications of liver cirrhosis. Currently, hepatic venous pressure gradient (HVPG) was the reference standard for evaluating portal pressure in patients with cirrhosis. However, the practice of HVPG is limited to require the extensive experience and highly specialized centers. In recent years, non-invasive methods were proposed to predict the degree of cirrhotic portal hypertension. Of them, liver stiffness measured by transient elastography had shown good performance for predicting clinically significant portal hypertension. However, liver stiffness only has a good correlation with portal pressure in the early stage of portal hypertension (HVPG<10 mmHg), because liver fibrosis is the main cause of portal hypertension in this period. In the stage of clinically significant portal hypertension (CSPH) (HVPG≥10 mmHg), increased portal vein inflow due to splanchnic vasodilation and hyperdynamic circulation, spleen stiffness may have a better correlation with HVPG than that of liver stiffness. Several studies have explored the combination of liver stiffness, platelet count and spleen stiffness for varices screening. However, there are few studies to report the above parameters for assessing CSPH and unneeded HVPG avoiding.

Since the spleen was stiffer than the liver, the current vibration-controlled transient elastography examination is dedicated to the liver, rather than the spleen. Very recently, a novel spleen-dedicated stiffness measured by transient elastography was proposed. The prospective, multicenter study (leaded by The First Hospital of Lanzhou University and Shulan (Hangzhou) Hospital) aims to add spleen stiffness as a supplementary parameter to establish new criteria for identify CSPH in patients with compensated cirrhosis, with a dedicated probe on transient elastography equipment to assess spleen stiffness and liver stiffness, and further develop a novel model based on spleen stiffness for predicting the liver decompensation in patients with compensated cirrhosis.

Study Design

Study Type:
Observational
Anticipated Enrollment :
300 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
A Combined Model Based on Spleen Stiffness, Liver Stiffness and Platelets for Assessing Portal Hypertension in Compensated Cirrhosis: A Prospective, Multicenter Study (CHESS2202)
Actual Study Start Date :
Sep 28, 2021
Anticipated Primary Completion Date :
Sep 27, 2022
Anticipated Study Completion Date :
Sep 27, 2022

Arms and Interventions

Arm Intervention/Treatment
Training cohort

Patients were fulfilled diagnosis of compensated cirrhosis based on radiological, histological features of liver cirrhosis and clinical manifestations.

Diagnostic Test: Hepatic venous pressure gradient
All patients underwent measurement of HVPG under local anesthesia.

Validation cohort

Patients were fulfilled diagnosis of compensated cirrhosis based on radiological, histological features of liver cirrhosis and clinical manifestations.

Diagnostic Test: Hepatic venous pressure gradient
All patients underwent measurement of HVPG under local anesthesia.

Outcome Measures

Primary Outcome Measures

  1. Accuracy of a new model based on spleen stiffness (kPa), liver stiffness (kPa) or platelets (/L) for assessing portal hypertension in compensated cirrhosis. [1 years]

    In HVPG (mmHg) as reference method in evaluating portal pressure measured by intervention specialist, to develop a new model based on spleen stiffness (kPa), liver stiffness (kPa) or platelets (/L) and evaluate the accuracy in diagnosing portal hypertension. Spleen stiffness (kPa) and liver stiffness (kPa) are measured by transient elastography with a dedicated probe.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. age above or equal to 18-year-old

  2. fulfilled diagnosis of compensated cirrhosis based on radiological, histological features of liver cirrhosis and clinical manifestations

  3. without decompensated events (e.g. ascites, bleeding, or overt encephalopathy)

  4. with spleen stiffness and liver stiffness by a dedicated probe on transient elastography examination and platelet count measurement

  5. with HVPG measurement

  6. signed informed consent

Exclusion Criteria:
  1. non-cirrhotic portal hypertension

  2. accepted primary prevention (non-selective beta blockers or endoscopic variceal ligation)

  3. lactation or pregnancy

  4. suspicious or confirmed hepatocellular carcinoma

  5. asplenia or splenectomy

  6. incomplete clinical information

Contacts and Locations

Locations

Site City State Country Postal Code
1 The First Hospital of Lanzhou University Lanzhou Gansu China 730000
2 The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School Nanjing Jiangsu China 210000
3 Qufu People's Hospital Jining Shandong China 272000
4 The Third People's Hospital of Taiyuan Taiyuan Shanxi China 030000
5 Shulan (Hangzhou) Hospital Hangzhou Zhejiang China 310000

Sponsors and Collaborators

  • Hepatopancreatobiliary Surgery Institute of Gansu Province
  • LanZhou University
  • Shulan Hospital of Hangzhou
  • The Third People's Hospital of Taiyuan
  • QuFu People's Hospital
  • The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School

Investigators

  • Study Chair: Lanjuan Li, M.D., Shulan Hospital of Hangzhou
  • Principal Investigator: Xiaolong QI, M.D., LanZhou University
  • Study Director: Huadong Yan, M.D., Shulan Hospital of Hangzhou

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Xiaolong Qi, Prof., Hepatopancreatobiliary Surgery Institute of Gansu Province
ClinicalTrials.gov Identifier:
NCT05251272
Other Study ID Numbers:
  • CHESS2202
First Posted:
Feb 22, 2022
Last Update Posted:
Jun 2, 2022
Last Verified:
Feb 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Xiaolong Qi, Prof., Hepatopancreatobiliary Surgery Institute of Gansu Province
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 2, 2022