Actively Recruiting

Age: 18Years - 75Years
All Genders
ID06205992

Three-dimensional MR Elastography and Two-dimensional MR Elastography for Assessing Cirrhosis and Portal Hypertension: A Prospective Multicenter Study

Led by Shengjing Hospital · Updated on 2026-02-09

100

Participants Needed

1

Research Sites

17 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating new non-invasive methods to predict hepatic venous pressure gradient (HVPG), a key measure in managing portal hypertension in cirrhosis. This study compares three-dimensional magnetic resonance elastography (3D-MRE) with two-dimensional magnetic resonance elastography (2D-MRE) to develop a risk stratification system that can guide personalized treatment for portal hypertension. Cirrhosis and portal hypertension pose significant health challenges, making less invasive diagnostic tools important for patient care. Participants will undergo imaging using either 3D-MRE or 2D-MRE, both performed on a 3.0-T MRI system with an eight-channel body coil. The study features two groups: one developing a model using 3D-MRE and a control group using 2D-MRE. Hepatic venous pressure gradient measurements are taken by trained radiologists following standard procedures. Comparing these imaging techniques aims to evaluate their accuracy in assessing portal hypertension. During the study, participants will have imaging and HVPG measurements within one month to ensure data consistency. Researchers will assess the accuracy of 3D-MRE and 2D-MRE features for predicting portal hypertension over a 12-month period. The study monitors participants through these diagnostic tests and evaluates how well the imaging models can predict HVPG, contributing to safer, more convenient management of cirrhosis-related complications.

CONDITIONS

Brief Title

3D-MRE and 2D-MRE for Assessing Cirrhosis and Portal Hypertension

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age over 18 years
  • Confirmed cirrhosis by laboratory tests, imaging, and clinical symptoms
  • Underwent 3D-MRE and 2D-MRE imaging within 1 month prior to HVPG measurement
  • Provided written informed consent
Not Eligible

You will not qualify if you...

  • Previous liver or spleen surgery
  • Liver cancer or chronic acute liver failure
  • Acute portal hypertension
  • Unreliable HVPG, 3D-MRE, or 2D-MRE results due to technical reasons
  • Received liver interventional therapy between HVPG and MRE imaging

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

Duration - Within 1 month

Participants undergo imaging studies using 3D-MRE and 2D-MRE and have hepatic venous pressure gradient (HVPG) measurements taken by trained radiologists to assess portal hypertension in cirrhosis.

1 to 2 visits depending on imaging and HVPG scheduling

Long-term Monitoring

Duration - 12 months

Participants are observed for up to 12 months to evaluate the accuracy of 3D-MRE and 2D-MRE features in assessing portal hypertension in cirrhosis.

Follow-up visits as scheduled for up to 12 months

Trial Site Locations

Total: 1 location

1

Shengjing Hospital of China Medical University

Shenyang, Liaoning, China, 110004

Actively Recruiting

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Research Team

Y

Yu Shi

Z

Zhiying Wang

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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Published Research Related To This Trial

An imaging-based artificial intelligence model for non-invasive grading of hepatic venous pressure gradient in cirrhotic portal hypertension.

Qian Yu, Yifei Huang, Xiaoguo Li...

https://pubmed.ncbi.nlm.nih.gov/35492878