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MR-based Models for Clinically Significant Portal Hypertension in Cirrhosis (CHESS1802)

MR-based Models for Noninvasive Detection of Clinically Significant Portal Hypertension in Cirrhosis (CHESS1802)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03766880
Enrollment
175
Registered
2018-12-06
Start date
2018-12-04
Completion date
2019-04-30
Last updated
2019-08-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension, Portal

Keywords

clinically significant portal hypertension, hepatic venous pressure gradient, MR imaging

Brief summary

Clinically significant portal hypertension (CSPH) is associated with an incremental risk of esophageal varices and overt clinical decompensations in cirrhosis. However, hepatic venous pressure gradient (HVPG) measurement, the gold standard for defining CSPH (HVPG≥ 10mmHg) is invasive and therefore not suitable for routine clinical practice. This is a multi-center diagnostic trial conducted at high-volume liver centres designed to determine the accuracy of MR-based models (investigational technology) for noninvasive detection of a CSPH in patients with cirrhosis. Transjugular HVPG measurement by means of catheterization of a hepatic vein with a balloon catheter is the gold-standard method to assess the presence of CSPH.

Detailed description

Clinically significant portal hypertension (CSPH) is associated with an incremental risk of esophageal varices and overt clinical decompensations in cirrhosis. However, hepatic venous pressure gradient (HVPG) measurement, the gold standard for defining CSPH (HVPG≥ 10mmHg) is invasive and therefore not suitable for routine clinical practice. This is a multi-center diagnostic trial conducted at high-volume liver centres (Zhongda Hospital, Medical School of Southeast University; Affiliated Lishui Hospital of Zhejiang University; Shandong Provincial Hospital affiliated to Shandong University; Beijing 302 Hospital; Xingtai People's Hospital; Shunde Hospital, Southern Medical University; The First Hospital of Zhengzhou University; Shanghai Public Health Clinical Center, Fudan University; The First Hospital of Lanzhou University; Nanfang Hospital of Southern Medical University; Ankara University School of Medicine) designed to determine the accuracy of MR-based models (investigational technology) for noninvasive detection of a CSPH in patients with cirrhosis. Transjugular HVPG measurement by means of catheterization of a hepatic vein with a balloon catheter is the gold-standard method to assess the presence of CSPH.

Interventions

PROCEDURETransjugular HVPG measurement

By means of catheterization of a hepatic vein with a balloon catheter.

PROCEDUREMR imaging

MR images for the post-processing analysis

Sponsors

Zhongda Hospital
CollaboratorOTHER
Beijing 302 Hospital
CollaboratorOTHER
Affiliated Lishui Hospital of Zhejiang University
CollaboratorUNKNOWN
Shandong Provincial Hospital
CollaboratorOTHER_GOV
Xingtai People's Hospital
CollaboratorOTHER
The First Hospital of Zhengzhou University
CollaboratorUNKNOWN
Shanghai Public Health Clinical Center, Fudan University
CollaboratorUNKNOWN
LanZhou University
CollaboratorOTHER
Southern Medical University, China
CollaboratorOTHER
Ankara University
CollaboratorOTHER
Nanfang Hospital, Southern Medical University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Age 18-75 years * With written informed consent * Confirmed liver cirrhosis based on liver biopsy or clinical findings * Scheduled to undergo clinically-indicated transjugular HVPG measurement by means of catheterization of a hepatic vein with a balloon catheter * Has undergone\> MR imaging within 14 days to hepatic vein catheterization * No hepatic-portal vein interventional therapy between MR imaging and hepatic vein catheterization

Exclusion criteria

* A contraindication to MR imaging, in particular pacemakers or implantable defibrillators, cochlear implants, neurosurgical clips, intra-orbital or brain metallic foreign bodies, endo prothesis since less than 4 weeks or osteosynthesis material since less than 6 weeks * Unable to comply with breathing or other imaging related instructions resulting in inability to obtain diagnostic quality MR imaging studies * Contraindication to the injection of contrast agent: pregnancy, lactation, history of allergic reaction to contrast agent injection. * Prior transjugular intrahepatic portosystem stent-shunt surgery * Prior devascularization operation * Has received a liver transplant * Any active, serious, life-threatening disease

Design outcomes

Primary

MeasureTime frameDescription
Diagnostic Performance of MR-based Models1 dayAccuracy, sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) of MR-based models for noninvasive detection of CSPH when compared to HVPG as the reference standard.

Countries

China, Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 28, 2026