Official Title: “A Clinical Study of the Efficacy of Esomeprazole or Rabeprazole on the Pattern of Release of Pro- and Anti-Inflammatory Cytokines From Gastric Mucosa of Patients With Peptic Ulcer Disease”

Although all PPIs are effective, there are some differences in their clinical performance, particularly in terms of the degree and speed of gastric acid suppression. Few data are also available about their effect of the pathophysiological mechanisms of gastritis and peptic ulcer disease. Aim of the present study is to investigate the effect of therapy with esomaprazole or rabeprazole on the mechanism of pathogenesis of gastritis and particularly on the pattern of release of pro- and anti- inflammatory cytokines associated to peptic ulcerative process by the gastric mucosa.

Study Type: Observational

Study Design: Natural History, Longitudinal, Defined Population, Prospective Study

Although all PPIs are effective, there are some differences in their clinical performance, particularly in terms of the degree and speed of gastric acid suppression. Few data are also available about their effect of the pathophysiological mechanisms of gastritis and peptic ulcer disease.

Triggering receptor expressed on myeloid cells (TREM)-1 is a recently discovered receptor expressed on the surface of neutrophils and monocytes. Engagement of TREM-1 has been reported to trigger the synthesis of proinflammatory cytokines. A soluble form of TREM-1, named sTREM-1, was observed and identified at significant levels in serum samples from patients with disease of the gastrointestinal tract inflammatory bowel disease. rendering interest about the implication of sTREM-1 in their pathogenesis.

sTREM-1 was also found elevated in the gastric juice of patients with peptic ulcer disease being correlated to the degree of the infiltration of the gastric mucosa by neutrophils.

Published data of our group elicit that sTREM-1 secretion is a crucial parameter for evolution from chronic gastritis to peptic ulcer disease. Samples of biopsies of gastric mucosa were cultured in the absence/presence of endotoxins showing that the inflamed mucosa was a potent secretor of sTREM-1 whatever ceased to exist post-antisecretory treatment.

Aim of the present study is to investigate the effect of therapy with esomaprazole or rabeprazole on the mechanism of pathogenesis of gastritis and particularly on the pattern of release of pro- and anti- inflammatory cytokines associated to peptic ulcerative process by the gastric mucosa.

Intervention(s) in this Clinical Trial

• Procedure: Endoscopy of upper GI tract
  • upper GI endoscopy, one time on diagnosis and a second time 15 days after the end of the treatment. Gastric juice will be aspirated immediately after the entrance of the endoscope into the gastric lumen. Four biopsy specimens will be obtained from adjacent areas of the gastric antrum. Each biopsy will be used for in vitro culture. Blood will be sampled from one antecubital vein under aseptic conditions. Each patient will be given antisecretory treatment and - if necessary- eradication treatment of H. pylori according to international guidelines.

Arms, Groups and Cohorts in this Clinical Trial

• Case: 1
  • A total of 130 patients with peptic ulcer disease and /or chronic gastritis will be enrolled in the study after written informed consent

Inclusion Criteria:

• Written informed consent.
• Abdominal pain or discomfort and/or
• Epigastric pain with nausea and vomiting and/or
• Dyspepsia.

Exclusion Criteria:

• Recent upper GI bleeding
• Gastric carcinoma
• Diabetes mellitus
• Liver cirrhosis
• Acute or chronic renal failure
• The ingestion of any antimicrobial or antisecretory medication for at least 15 days prior to endoscopy.

Gender Eligibility for this Clinical Trial: Both

Minimum Age for this Clinical Trial: 18 Years

Maximum Age for this Clinical Trial: N/A

Are Healthy Volunteers Accepted for this Clinical Trial?: No

Lead Sponsor: University of Athens

Overall Clinical Trial Officials and Contacts

Evangelos J. Giamarellos-Bourboulis, MD, PhD Study Chair 4th Department of Internal Medicine, ATTIKON University Hospital, 124 62 Athens, Greece  

Overall Contact: Evangelos J Giamarellos-Bourboulis, MD, PhD 00302105831000 giamarel@ath.forthnet.gr

Information obtained from ClinicalTrials.gov on September 05, 2008

Link to the current ClinicalTrials.gov record. http://clinicaltrials.gov/show/NCT00534443

Study ID Number: 3530

ClinicalTrials.gov Identifier: NCT00534443

Health Authority: Greece: National Organization of Medicines