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EUS Guided Portal-systemic Pressure Gradient Measurement to Predict Treatment Response and Outcomes of Varices to Endoscopic Variceal Ligation in Patients With Chronic Hepatitis.

Key facts

Where
Hong Kong, ChinaSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 75 years old?

Source: NCT05597488, who can take part

Where in China

  • Chinese University of Hong KongHong Kong, ChinaContact: Anthony Y Teoh, FRCSEd(Gen)Taking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

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Trial details

Who runs it
Chinese University of Hong Kong
Trial code
NCT05597488
Record updated
20 March 2026
Original description
The aim of the current study is to assess if EUS-PPGM could predict the treatment response and outcomes of varices to endoscopic variceal ligation (EVL) in patients with chronic hepatitis. The hypothesis is that a high EUS-PPGM value at 3 months correlates with the presence of varices requiring EVL in patients that have received primary or secondary variceal prophylaxis on 1 year follow-up upper endoscopy.Read full original descriptionShow less

The aim of the current study is to assess if EUS-PPGM could predict the treatment response and outcomes of varices to endoscopic variceal ligation (EVL) in patients with chronic hepatitis. The hypothesis is that a high EUS-PPGM value at 3 months correlates with the presence of varices requiring EVL in patients that have received primary or secondary variceal prophylaxis on 1 year follow-up upper endoscopy.

Inclusion: Age between 18 to 75 years old; Informed consent available; Suffering from chronic hepatitis induced cirrhosis; Suffering from oesophageal varices and received EVL as a result of; Primary variceal prophylaxis during a variceal surveillance program on oesophagogastroduodenoscopy (OGD) or; Secondary variceal prophylaxis after EVL in patients with active oesophageal variceal bleeding; Or bleeding gastric varices that have received endoscopic canoacrylate injection.

Exclusion: Anatomical Main portal vein thrombosis Anatomic alterations of the hepatic vasculature that prevent access to the portal vein or intrahepatic portion of the hepatic veins (identified at screening and/or during the endoscopic procedure); Previous history of spontaneous bacterial peritonitis within the previous three months Portopulmonary hypertension Cardiac decompensation; Endoscopically Confirmed Exclusion Criteria Presence of ascites in the path of the needle that prevents apposition of the gastrointestinal tract and liver; Presence of gastric or duodenal ulcers, dieulafoy's lesion or cancers; Medical Child-Pugh Class C Uncorrected platelet count <50,000 INR > 1.5 (natural) History of hepatic encephalopathy Current or history of hepatocellular carcinoma.

ClinicalTrials.gov NCT05597488