The Role of CYP2C19 on the Eradication of H. Pylori Infection:Implication of PK/PD Relationships
Information source: National Taiwan University Hospital
Information obtained from ClinicalTrials.gov on June 20, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Peptic Ulcer With H. Pylori Infection; Gastritis With H. Pylori Infection
Intervention: Rabeprazole vs. Esomeprazole (Drug)
Phase: N/A
Status: Active, not recruiting
Sponsored by: National Taiwan University Hospital Official(s) and/or principal investigator(s): Jyh-Chin Yang, M.D., Principal Investigator, Affiliation: Department of Internal Medicine, National Taiwan University Hospital
Summary
The objective of this trial is to find the rationale and the optimal dose and duration of
regimen for the eradication of H. pylori infection using different proton pump inhibitors.
Clinical Details
Official title: The Role of CYP2C19 Poor Metabolizers and Extensive Metabolizers of PPI in Short-Term Triple Therapy on the Eradication of H. Pylori Infection: Implication of PK/PD Relationships
Study design: Treatment, Randomized, Open Label, Dose Comparison, Crossover Assignment, Pharmacokinetics Study
Primary outcome: the role of CYP2C19 on the eradication of H. pylori infection
Secondary outcome: implication of PK/PD relationships
Detailed description:
Helicobacter pylori in known to be closely associated with the pathogenesis of gastroduodenal
disorders such as peptide ulcer. Eradication of this bacterium is important in the treatment
of these diseases as well as in the reduction of the recurrence. The one-week triple therapy
with proton pump inhibitors (PPIs) is now considered to be the standard therapies in the
treatment of Helicobacter pylori infection, providing more than 80% eradication rates with
few adverse effects. PPIs are mainly metabolized by CYP2C19, which is known to exhibit
polymorphisms in both its genotype and phenotype. Based on the PK/PD results of our study on
PPI, recently, we have proposed that CYP2C19 poor metabolizers might be subject to
advantageous conditions, especially after day-4, for the treatment of H. pylori infection
when 20 mg rabeprazole was given twice daily. Our results also suggest a possibility to start
the triple therapy on day-4 of rabeprazole treatment to ensure the optimal acid suppression
effect for antibiotics to exert the bacteriocidal effect. To find the rationale and the
optimal dosing regimen for the eradication of H. pylori infection using different proton pump
inhibitors, volunteers of four groups would be included in this study. PPI (rabeprazole or
esomeprazole) is given for 7 days. Antibiotics are given starting from day-1 or day-4 of PPI
dosing. The eradication rate of H. pylori infection and the PK/PD of PPIs are also
evaluated.
Eligibility
Minimum age: 18 Years.
Maximum age: N/A.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Male and female dyspeptic patients with H. pylori-positive peptic ulcer or gastritis
will be recruited at the university hospital in this study.
Exclusion Criteria:
- 1)Pregnant or lactating female;*2)Patients have endoscopy-based evidence of gastric
malignancy, pyloric obstruction, and esophageal stricture requiring dilation, fresh
clot, active bleeding, or perforated ulcers;3)Patients requiring anticoagulants or
corticosteroid therapy (at dosages greater than the equivalent of prednisone, 10
mg/day);4)Patients with significant impairment of renal function (creatinine>2mg/dl);
liver function impairment (AST and ALT 2x upper limit of normal); severe cardiac
disease, e. g. angina pectoris, myocardial infarction, cardiac arrhythmia, congestive
heart failure (New York Heart Association Functional Classification III and IV) or
acute respiratory disease;5)Patients with a history of esophageal and/or gastric
varices;6)Use of other investigational drugs within 30 days prior to the study.
Locations and Contacts
Department of Internal Medicine, National Taiwan University Hospital, Taipei 100, Taiwan
Department of Internal Medicine, National Taiwan University Hospital, Taipei 100, Taiwan
Additional Information
Starting date: June 2004
Ending date: April 2005
Last updated: November 22, 2005
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