ClinicalTrials.Veeva

Menu

A Multi-center Study for Eradication of Refractory Helicobacter Pylori

T

Taizhou Hospital

Status

Unknown

Conditions

Gastritis

Treatments

Device: The result of 13C-urea breath test after treatment based on the selection of clarithromycin, levofloxacin, metronidazole, amoxicillin,tetracycline,furazolidone and the dose of esomeprazole
Device: The result of H pylori culture based on gram staining and enzyme activity testing
Device: The result of Amoxicillin resistance in vitro based on antibiotic susceptibility testing

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT02741414
TaizhouH

Details and patient eligibility

About

Recently studies showed that the eradication rate of H. pylori fail to exceed 80% and even falls into an unacceptable range. A major cause of treatment failure is associated with antibiotic resistance and poor patient compliance. However, the refractory infection of H. pylori is still existing, although patients have good compliance and receive standardized treatment. This phenomenon is likely attributed to the different ratio of sensitive and resistance in H. pylori, the difference of Amoxicillin resistance between in vivo and in vitro, the difference between phenotype and genotype or the influence of micro-environment in the stomach. In order to solve the refractory infection of H. pylori, investigators performed a muti-center study together with other 14 institutions. In this study, investigators will select the patients with refractory infection of H. pylori after two standardized treatment from patients with first eradication therapy of H. pylori infection. Then, investigators will perform a high-throughput sequencing for patients in groups. Finally, investigators will compare the differences between the patients with first successful eradication and patients with refractory infection of H. pylori, such as drug resistance gene mutation, phenotype and genotype, the mechanisms of Amoxicillin resistance and micro-environment in stomach.

Enrollment

4,428 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age 18~70 years old, male or female, the first eradication therapy of H. pylori infection patients.
  2. Symptoms of abdominal pain, bloating, acid efflux, belching, nausea, vomiting, heartburn, chest pain, vomiting, melena, etc.
  3. Unused antibiotics, bismuth, H2 receptor antagonists or PPIs by nearly 4 weeks
  4. 13C-labelled urea breath test positive.
  5. Agreed to Helicobacter pylori culture and sensitivity testing taken by endoscopy gastric biopsy specimens,and the result of culture was positive.
  6. Agreed to Helicobacter pylori eradication therapy and cooperate with the eradication efficacy follow-up survey.

Exclusion criteria

  1. Severe heart, liver, kidney dysfunction.
  2. Pregnant or lactating women.
  3. Complications of bleeding, perforation, pyloric obstruction, cancer.
  4. Esophageal,gastrointestinal surgery history.
  5. Patients can not properly express their complaints,such as psychosis, severe neurosis.
  6. Taking nonsteroidal antiinflammatory drugs (NSAIDs) or alcohol abusers.
  7. Allergic to penicillin or either drugs of the 6 antibiotic tested by susceptibility testing.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

4,428 participants in 3 patient groups

H pylori culture negative group
Experimental group
Description:
The patients who have the negative result of H pylori culture were classified into H pylori culture negative group.
Treatment:
Device: The result of H pylori culture based on gram staining and enzyme activity testing
The first successful eradication group
Experimental group
Description:
The patients with first eradication therapy of H. pylori infection have the first successful treatment based on the standardized treatment including antibiotics selection from antibiotic susceptibility testing and proton pump inhibitors (PPIs) dose selection from CYP2C19 gene sequencing.
Treatment:
Device: The result of H pylori culture based on gram staining and enzyme activity testing
Device: The result of Amoxicillin resistance in vitro based on antibiotic susceptibility testing
Device: The result of 13C-urea breath test after treatment based on the selection of clarithromycin, levofloxacin, metronidazole, amoxicillin,tetracycline,furazolidone and the dose of esomeprazole
The refractory infection of H. pylori group
Experimental group
Description:
The patients with first eradication therapy of H. pylori infection have the two failure treatment based on the standardized treatment including antibiotics selection from antibiotic susceptibility testing and PPIs dose selection from CYP2C19 gene sequencing.
Treatment:
Device: The result of H pylori culture based on gram staining and enzyme activity testing
Device: The result of Amoxicillin resistance in vitro based on antibiotic susceptibility testing
Device: The result of 13C-urea breath test after treatment based on the selection of clarithromycin, levofloxacin, metronidazole, amoxicillin,tetracycline,furazolidone and the dose of esomeprazole

Trial contacts and locations

1

Loading...

Central trial contact

Liping Ye, BSc

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems