Ultrasound Prediction of Esophageal Variceal Bleeding Risk

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorAssiut University

About this trial

This prospective observational study aims to evaluate the accuracy of using routine abdominal ultrasound to predict the risk of esophageal variceal bleeding in adult patients with liver cirrhosis. Esophageal variceal bleeding is a serious complication of chronic liver disease. While upper gastrointestinal endoscopy is the current standard for diagnosing and grading these varices, it is an invasive procedure.

In this study, researchers will use ultrasound to measure the patient's spleen size and portal vein diameter. These non-invasive measurements will then be compared to the results of a standard upper endoscopy performed within 48 to 72 hours. The goal is to determine if these simple ultrasound measurements can reliably predict the presence, grade, and bleeding risk of esophageal varices, which could potentially reduce the need for routine invasive endoscopic screenings in the future.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adult patients (age ≥18 years) with chronic liver disease and clinical/laboratory/radiological evidence of liver cirrhosis

Both compensated and decompensated cirrhosis (Child-Pugh classes A, B, and C)

Patients scheduled for upper gastrointestinal endoscopy

Patients who provide informed consent

Disqualifiers

Previous history of endoscopic variceal band ligation or sclerotherapy

Prior surgical portosystemic shunt procedures or transjugular intrahepatic portosystemic shunt (TIPS)

Hepatocellular carcinoma with portal vein thrombosis

Previous splenectomy

Trial population

Adult patients (aged 18 years and older) with chronic liver disease and established liver cirrhosis (including both compensated and decompensated, Child-Pugh classes A, B, and C) who are scheduled for an upper gastrointestinal endoscopy at AL-Rajhi University Hospital, Assiut University, Egypt.

Trial design

Design model

Cohort

Time perspective

Cross-sectional

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Grade of esophageal varices

Assessed during upper gastrointestinal endoscopy and classified according to the General Rules for Recording Endoscopic Findings: Grade I (small, straight varices), Grade II (enlarged, tortuous varices occupying \<1/3 of lumen), and Grade III (large, coil-shaped varices occupying \>1/3 of lumen).

Time frame
Baseline (at the time of upper gastrointestinal endoscopy, performed within 48 to 72 hours of the ultrasound examination)

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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