RecruitingPhase 1Phase 2NCT06302049

Clinical Study Evaluating the Safety and Efficacy of Esomeprazole in Treatment of Non-alcoholic Steatohepatitis

Clinical Study Evaluating the Safety and Efficacy of Esomeprazole in Treatment of Non-alcoholic Steatohepatitis: A Randomized Controlled Trial.


Sponsor

Sadat City University

Enrollment

46 participants

Start Date

Jun 1, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The aim of the study is to test the implication of esomeprazole as a possible potential therapy for patients with NASH through evaluating its effect on ultrasound and fibrosis risk scores, serum levels of liver fibrosis biomarkers (fibronectin 1), insulin resistance, metabolic and inflammatory parameters.


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Inclusion Criteria6

  • Both males and females.
  • Diabetic and non-diabetic patients.
  • Age >18 years old.
  • Overweight and obese patient: Body mass index (BMI) ≥ 25 kg/ m2 but <40 kg/ m2.
  • Patients with heartburn, peptic ulcer, gastrointestinal reflux disease, erosive esophagitis, Zollinger-Ellison syndrome and helicobacter pylori infection.
  • Patients with established diagnosis of NASH based on liver ultrasonography, mild to moderate elevation in aminotransferase activities (>2 but <5 times upper limit of normal), hepatic steatosis index (HIS) >36, HAIR score of 2 or 3.

Exclusion Criteria9

  • Patients with a history of hypersensitivity to esomeprazole.
  • Patients with BMI ≥ 40 kg/ m2.
  • Patients taking warfarin, clopidogrel, digoxin, diazepam and phenytoin to avoid drug-drug interactions as these drugs are CYP2C19 substrates.
  • Patients infected with human immune deficiency virus taking antiretroviral medicines or dosage forms containing rilpivirine.
  • Patients with a history of viral hepatitis, autoimmune hepatitis, sclerosing cholangitis, biliary obstruction, primary biliary cirrhosis, hemochromatosis, Wilson's disease and alpha-1 antitrypsin deficiency.
  • Patients on medications associated with steatosis such as NSAIDs, amiodarone, tamoxifen, estrogen, sodium valproate, corticosteroids, and methotrexate.
  • Patients with cancer or with a history of cancer.
  • Patients with cardiovascular diseases.
  • Pregnant and lactating females

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGEsomeprazole

esomeprazole 20 mg once daily

DRUGPlacebo

Placebo once daily


Locations(1)

National Liver Institute

Shibīn al Kawm, Egypt

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06302049


Related Trials