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Recruiting NCT05475015

NCT05475015 3D-MRE for Assessing Cirrhosis, Advanced Chronic Liver Disease and Portal Hypertension

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Clinical Trial Summary
NCT ID NCT05475015
Status Recruiting
Phase
Sponsor Shengjing Hospital
Condition Cirrhosis, Liver
Study Type OBSERVATIONAL
Enrollment 150 participants
Start Date 2022-08-16
Primary Completion 2026-07-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 75 Years
Study Type OBSERVATIONAL
Interventions
3D-MREHVPG

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 150 participants in total. It began in 2022-08-16 with a primary completion date of 2026-07-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

How to construct a novel, non-invasive, accurate, and convenient method to achieve prediction of hepatic venous pressure gradient (HVPG) is an important general problem in the management of portal hypertension in cirrhosis or advanced chronic liver disease. We plan to investigate the ability of three demensional-magnetic resonance elastography (3D-MRE) to establish a risk stratification system and perform tailored management for portal hypertension in cirrhosis or advanced chronic liver disease.

Eligibility Criteria

Inclusion criteria were: (1) ≥18 years; (2) written informed consent; (3) confirmed ACLD of any liver disease etiology; (4) clinically indicated for HVPG measurement, with 3D-MRE performed within one month prior. Exclusion criteria were: (1) hepatic or extrahepatic malignancies, or large hepatic or splenic focal diseases affecting MRE measurement; (2) MR or HVPG contraindications; (3) prior liver or splenic surgery affecting MRE measurement; (4) treatment with nonselective β-blockers (NSBB) between MRE and HVPG measurements; (5) invalid or unreliable HVPG or MRE results and (6) biliary obstruction or dilation on MR images.

Contact & Investigator

Central Contact

Yifei Huang, M.D.

✉ huangyf1995@foxmail.com

📞 +86 158 0000 4518

Principal Investigator

Yu Shi, Prof.

PRINCIPAL INVESTIGATOR

Shengjing Hospital

Frequently Asked Questions

Who can join the NCT05475015 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 75 Years, studying Cirrhosis, Liver. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05475015 currently recruiting?

Yes, NCT05475015 is actively recruiting participants. Contact the research team at huangyf1995@foxmail.com for enrollment information.

Where is the NCT05475015 trial being conducted?

This trial is being conducted at Shenyang, China.

Who is sponsoring the NCT05475015 clinical trial?

NCT05475015 is sponsored by Shengjing Hospital. The principal investigator is Yu Shi, Prof. at Shengjing Hospital. The trial plans to enroll 150 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology