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Portal Pressure Gradient (PPG) Measurement Guided by Endoscopic Ultrasound (EUS)NCT06994039

Left Lateral Position and Supine Position in EUS-PPG Measurement

An observational study of Portal Pressure Gradient (PPG) Measurement Guided by Endoscopic Ultrasound (EUS) and Left Lateral Decubitus, run by Second Affiliated Hospital, Zhejiang University, School of Medicine at 1 site in China.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The consistency of EUS-PPG measurements between left lateral decubitus and supine positions is unclear. In this prospective comparative study, we are aimed to evaluate the correlation between EUS-PPG measured in supine position (EUS-suPPG), and EUS-PPG measured in left lateral decubitus position (EUS-lePPG). Read more about this study

Who is it for?
Ages 18 to 80 years
What is being tested?
EUS-lePPG
Type of treatment
Surgery or procedure
How many people
30 participants
Where
1 siteChina
Study dates
16 Jun 2025to 29 Dec 2025
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Hospitalized patients with liver cirrhosis

Who may be able to join

  • Hospitalized patients with liver cirrhosis, and are willing to sign the informed consent.

Who cannot join

  • Unwilling to sign the informed consent
  • Severe coagulopathy (INR>1.6)
  • Severe thrombocytopenia (platelets <20,000/μL)
  • Bacteremia
  • Age<18, or≥81
  • Pregnancy

Trial locations and contacts

1 site in 1 country.

China1 site
  • The 2nd Affiliated Hospital, School of Medicine, Zhejiang University

    Hangzhou

Other trials in China

About this study

Official title: The Comparative Study on Left Lateral Position and Supine Position in Endoscopic Ultrasound Guided Portal Pressure Gradient Measurement

The consistency of EUS-PPG measurements between left lateral decubitus and supine positions is unclear. In this prospective comparative study, we are aimed to evaluate the correlation between EUS-PPG measured in supine position (EUS-suPPG), and EUS-PPG measured in left lateral decubitus position (EUS-lePPG).

Read the detailed description

The hepatic venous pressure gradient (HVPG) remains the gold standard for assessing portal hypertension, yet its clinical application faces several limitations. First, HVPG has restricted diagnostic scope, being unable to accurately evaluate prehepatic or presinusoidal portal hypertension. Second, the measurement process exposes both patients and physicians to radiation and involves complex techniques that preclude routine implementation in many hospitals. Finally, as HVPG indirectly estimates portal pressure through wedged hepatic venous pressure, its accuracy may be compromised by multiple factors including intrahepatic venous shunting, catheter insertion depth, excessive sedation or patient agitation during the procedure, and incomplete balloon occlusion of hepatic venous flow.

Endoscopic ultrasound-guided portal pressure gradient (EUS-PPG) measurement effectively addresses these limitations of HVPG. Current clinical studies on EUS-PPG have predominantly been conducted in the supine position. However, this position significantly increases the technical difficulty of endoscopic ultrasonography and complicates the simultaneous performance of endoscopic selective varices devascularization (EUS-ESVD) under single anesthesia. The consistency of EUS-PPG measurements between left lateral decubitus and supine positions requires further investigation.

This prospective comparative study enrolls hospitalized patients with liver cirrhosis. EUS-guided puncture of both the portal vein and hepatic vein were performed using a 25G needle. Pressure transducers measure the portal venous pressure (PVP) and hepatic venous pressure (HVP), with their differential defined as EUS-PPG. Measurements obtained in supine position are designated EUS-suPPG, while those in left lateral decubitus position are termed EUS-lePPG. Statistical analysis will evaluate the correlation between EUS-suPPG and EUS-lePPG values, with postoperative monitoring for complications including infection and hemorrhage.

Being tested
EUS-lePPG

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • EUS-lePPGProcedure or surgery

    EUS-PPG measured in left lateral decubitus position

Study groups in NCT06994039
Study groupRoleWhat they receive
EUS-suPPGEUS-PPG measured in supine position
Receives: Procedure: EUS-lePPG

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. EUS-lePPG

    EUS-PPG measured in left lateral decubitus position

    Measured: From the begining of zero calibration for pressure transducer to the end of the endoscopic procedure, until up to 1 day.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 May 2025
  2. Study start16 Jun 2025
  3. Primary completion29 Dec 2025
  4. Study completion29 Dec 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case only
Time perspective
Prospective
Enrolment
30 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06994039
Sponsor's protocol ID
2025-0729
Status last verified
May 2025
First submitted
20 May 2025
Last updated
6 Feb 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Portal Pressure Gradient (PPG) Measurement Guided by Endoscopic Ultrasound (EUS) and Left Lateral Decubitus, run by Second Affiliated Hospital, Zhejiang University, School of Medicine at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 6 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

EUS-lePPG (time frame: From the begining of zero calibration for pressure transducer to the end of the endoscopic procedure, until up to 1 day.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Feb 2026.

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