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NCT06908798Recruiting

Fecal Calprotectin for Prediction of Esophageal Varices in Cirrhotic Patients

The Accuracy of Fecal Calprotectin in Detecting Esophageal Varices in Egyptian Patients With Liver Cirrhosis

Source: ClinicalTrials.gov · Last updated 3 Apr 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The goal of this cross-sectional observational study is to evaluate the accuracy of fecal calprotectin versus non-invasive scores in assessing the presence and grading of esophageal varices in Egyptian patients. Researchers will compare fecal calprotectin levels in cirrhotic patients with and without esophageal varices (EVs) and healthy subjects. researchers will also evaluate the performance of fecal calprotectin, AST to platelet ratio index (APRI) score, fibrosis-4 (FIB-4) score, albumin-bilirubin (ALBI) score, platelet-albumin-bilirubin (PALBI) score, and platelet-spleen diameter ratio (PSR) for predicting esophageal varices. Participants will undergo history-taking, clinical examination, laboratory investigations, fecal calprotectin, abdominal ultrasonography, and upper endoscopy. Endoscopic grading of esophageal varices will be done using Paquet's classification. The APRI, FIB-4, ALBI, PALBI, and PSR scores will be calculated. The performance of fecal calprotectin for predicting EVs will be compared versus other non-invasive scores.

Status (registry)
Recruiting
Study type
Observational
Enrollment
156 (estimated)
First submitted
27 Mar 2025
Start date
1 Dec 2024
Primary completion date
1 Dec 2025
Lead sponsor
Tanta University
NCT number
NCT06908798

What you commit to

  • Study type: Observational
  • Planned participants: 156
  • From 1 Dec 2024 to the primary completion date, 1 Dec 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients on proton pump inhibitors or NSAID.

Other illness

  • Inflammatory bowel disease.
  • Malignancy.

Age

  • Patients aged \< 18 years.

Other

  • Infectious gastroenteritis.
  • Patients with spontaneous bacterial peritonitis.
  • Patients with hepatic encephalopathy.
  • Unwilling to participate in our study.

Who the study is looking for

  • Age ≥18 years
  • Liver cirrhosis

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Tanta University Hospitals
Coordinator of this site? Confirm its status
TantaEgyptRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.