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Duodenal UlcerPhase 4NCT00854451

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

A Phase 4 study testing omeprazole plus amoxicillin in people with Duodenal Ulcer and Helicobacter Pylori Infection, run by National Taiwan University Hospital at 1 site in Taiwan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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)… Read more about this study

Who is it for?
Ages 20 to 75 years
Conditions the study is for
Duodenal Ulcer, Helicobacter Pylori Infection
What is being tested?
omeprazole plus amoxicillin
Could I receive a placebo?
No, everyone receives an active treatment
How many people
128 participants
Where
1 siteTaiwan
Study dates
Aug 1996to Feb 1998
Phase
Phase 4
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 20 to 75 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

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

Who cannot join

  • 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.

Trial locations and contacts

1 site in 1 country.

Taiwan1 site
  • Department of Internal Medicine, National Taiwan University Hospital

    Taipei, 10043

Other trials in Taiwan

About this study

Official title: Relation of Metabolic Rate of Omeprazole and Eradication of Helicobacter Pylori Infection - A Combination of Clinical and Pharmacogenetic Study

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.

Being tested
omeprazole plus amoxicillin
Keywords
Helicobacter pylori, CYP2C19 genotype, intragastric pH, dual therapy, antibiotic resistance
Medical subject headings
Duodenal Ulcer

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • omeprazole plus amoxicillinDrug

  • omeprazole plus amoxicillinDrug

  • omeprazole plus amoxicillinDrug

  • omeprazole plus amoxicillinDrug

Study groups in NCT00854451
Study groupRoleWhat they receive
1 omeprazole plus amoxicillinActive comparatoromeprazole 20mg bid 2wk + amoxicillin 500mg qid 2wk
Receives: Drug: omeprazole plus amoxicillin
2 omeprazole plus amoxicillinActive comparatoromeprazole 20mg bid 2wk + amoxicillin 250mg qid 2wk
Receives: Drug: omeprazole plus amoxicillin
3 omeprazole plus amoxicillinActive comparatoromeprazole 20mg qd 2wk + amoxicillin 500mg qid 2wk
Receives: Drug: omeprazole plus amoxicillin
4 omeprazole plus amoxicillinActive comparatoromeprazole 20mg qd 2wk + amoxicillin 250mg qid 2wk
Receives: Drug: omeprazole plus amoxicillin

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Helicobacter pylori eradication rate and intragastric pH value

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted3 Mar 2009 (estimated)
  2. Study startAug 1996
  3. Primary completionDec 1997
  4. Study completionFeb 1998

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Investigator
Enrolment
128 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00854451
Sponsor's protocol ID
NSC86-2314-B002-169
Status last verified
Jul 1996
First submitted
6 Feb 2009
Last updated
3 Mar 2009
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing omeprazole plus amoxicillin in people with Duodenal Ulcer and Helicobacter Pylori Infection, run by National Taiwan University Hospital at 1 site in Taiwan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 3 Mar 2009. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Taiwan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Helicobacter pylori eradication rate and intragastric pH value. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Mar 2009.

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