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CompletedNCT00854451Updated Mar 3, 2009

Relation of Metabolic Rate of Omeprazole and Eradication of Helicobacter Pylori Infection

A Phase 4 interventional study of omeprazole plus amoxicillin and omeprazole plus amoxicillin in Duodenal Ulcer and Helicobacter Pylori Infection, sponsored by National Taiwan University Hospital. Completed at 1 site in Taiwan. Open to participants aged 20 Years to 75 Years. Per ClinicalTrials.gov, last updated 2009-03-03.

Sponsored by National Taiwan University Hospital · Phase 4, Interventional, and Treatment

Phase
Phase 4
Study type
Interventional
Enrollment
128
Allocation
Randomized
Ages
20 Years to 75 Years
Sex
All
01

Study summary

The aims of this study are (1) to evaluate the prevalence rate of PM of CYP2C19 in our country; (2) to evaluate the efficacy of dual therapy with different dose of omeprazole and amoxicillin; (3) to judge the relationship of genotype of CYP2C19 and the eradication rate of dual therapy in the peptic ulcer patients; (4) to try to find out a predictor of success of dual therapy and an optimal dose of dual therapy as first-line and rescue anti-Helicobacter pylori regimen.

Read the detailed description

Anti-H. pylori therapy is now recommended in patients with peptic ulcer disease associated with bacterial infection. Dual therapy containing one PPI and amoxicillin has been suggested to be a better treatment than classical triple therapy containing bismuth, metronidazole, and tetracycline for H. pylori eradication due to its better compliance and fewer side effects. However, the variation in the eradication rate among different studies has limited its clinical application. Nonetheless, the amoxicillin-based dual therapy, with very rare prevalence of primary and secondary antibiotic resistance, has the potential to be an optimal first-line and rescue anti-Helicobacter pylori regimen if the confounding factors that cause the labile treatment outcome can be clarified. Cytochrome P450 2C19(CYP2C19), the enzyme that metabolizes omeprazole, was found to have genetic polymorphism in its enzyme activity. The percentage of poor metabolizer(PM) of CYP2C19 was much higher in Oriental(18\~23%) comparing to Caucasian(3\~5%).

The aims of this study is to try to find out a predictor of success of dual therapy and an optimal dose of dual therapy as first-line and rescue anti-Helicobacter pylori regimen. About 130 patients with Hp positive duodenal ulcer will be enrolled and allocated randomly into one of four treatment groups:Group A:omeprazole 20mg bid 2wk + amoxicillin 500mg qid 2wk; Group B:omeprazole 20mg bid 2wk + amoxicillin 250mg qid 2wk; Group C:omeprazole 20mg qd 2wk + amoxicillin 500mg qid 2wk; Group D:omeprazole 20mg qd 2wk + amoxicillin 250mg qid 2wk. All patients will receive endoscopic exam with biopsy again within 1\~2 months after the end of treatment. The status of H. pylori infection was examined by endoscopy or the 13C-urea breath test (if the patients refused the second endoscopy). Biopsy from the antrum and body will be taken for the culture, histology and CLO test. Twenty-four hours intragastric pH measurements will be performed on 6 randomly selective patients of each group when these patients complete the first week course of treatment. PCR-RFLP method will be used to detect genotype of CYP2C19 polymorphism using the genomic DNA extracted from the whole blood in all 130 treated patients. The genotyping results will be correlated with the H. pylori eradication rate and intragastric pH value.

The equivalence of demographic information among various treatment groups or genotypes will be revealed by chi-square independence test, t-test, one-way ANOVA, or Kruskal-Wallis test. The above statistical methods as well as Mann-Whitney test will be also used to analyze clinical outcome. Confidence intervals for eradication rates will be computed by plus-four method. Multiple logistic regression will be used to explore the predictor of the eradication outcome. Multiple regression will be used to explore the predictor of the intragastric acidity. A p-value less than 0.05 will be considered statistically significant.

02

Conditions studied

  • Duodenal Ulcer
  • Helicobacter Pylori Infection

Keywords

  • Helicobacter pylori
  • CYP2C19 genotype
  • intragastric pH
  • dual therapy
  • antibiotic resistance
03

In context

Infections

6,688 studies on the registry are indexed under Infections; 807 are open to participants now.

This study's enrollment of 128 is close to the median of 120 across 4,201 interventional studies indexed under Infections.

Browse Infections studies →

Lead sponsor

National Taiwan University Hospital is the lead sponsor of 2,563 studies on the registry; 570 are open to participants now.

Of its 11 completed or terminated interventional studies of FDA-regulated products, 2 (18%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Male and female dyspeptic patients with H. pylori-positive duodenal ulcer.

Exclusion criteria

Exclusion Criteria:

  • Pregnant or nursing woman
  • Serious concomitant illness
  • Malignant tumor of any kind
  • Serious bleeding during the course of this ulcer
  • Previous gastric surgery
  • Taking bismuth compounds, proton pump inhibitors, antibiotic or non-steroid anti-inflammatory drugs for at least one month prior to pretreatment endoscopy.
05

Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Investigator)
Enrollment
128 participants (actual)

Study arms

  • Active comparator
    1 omeprazole plus amoxicillin

    omeprazole 20mg bid 2wk + amoxicillin 500mg qid 2wk

    Drug: omeprazole plus amoxicillin

  • Active comparator
    2 omeprazole plus amoxicillin

    omeprazole 20mg bid 2wk + amoxicillin 250mg qid 2wk

    Drug: omeprazole plus amoxicillin

  • Active comparator
    3 omeprazole plus amoxicillin

    omeprazole 20mg qd 2wk + amoxicillin 500mg qid 2wk

    Drug: omeprazole plus amoxicillin

  • Active comparator
    4 omeprazole plus amoxicillin

    omeprazole 20mg qd 2wk + amoxicillin 250mg qid 2wk

    Drug: omeprazole plus amoxicillin

Interventions

  • Drugomeprazole plus amoxicillin
  • Drugomeprazole plus amoxicillin
  • Drugomeprazole plus amoxicillin
  • Drugomeprazole plus amoxicillin
06

What researchers measure

Primary outcomes

  1. Helicobacter pylori eradication rate and intragastric pH value

07

Study locations

1 site
  • Department of Internal Medicine, National Taiwan University Hospital
    Taipei, 10043, Taiwan
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 3, 2009, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00854451
Lead sponsor
National Taiwan University Hospital
Collaborators
National Science Council, Taiwan
First posted
Mar 3, 2009
Start date
Aug 1996
Primary completion
Dec 1997
Completion
Feb 1998
Last update
Mar 3, 2009

Study contacts

Jyh-Chin Yang, M.D.
principal investigator · Department of Internal Medicine, National Taiwan University Hospital

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jul 1996. You cannot join it, but the record below documents what was studied.

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