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A Multi-center Study for Eradication of Refractory Helicobacter Pylori

Primary Purpose

Gastritis

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
The result of H pylori culture based on gram staining and enzyme activity testing
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 result of Amoxicillin resistance in vitro based on antibiotic susceptibility testing
Sponsored by
Taizhou Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gastritis focused on measuring Helicobacter pylori, Antibiotic resistance, Sequencing, Mechanism

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept 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.

Sites / Locations

  • Xianju People HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

H pylori culture negative group

The first successful eradication group

The refractory infection of H. pylori group

Arm Description

The patients who have the negative result of H pylori culture were classified into H pylori culture negative group.

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.

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.

Outcomes

Primary Outcome Measures

The eradication rate of H. pylori reach to 95% in all groups
The microflora structure of a total of 240 patients in the first successful eradication group and the refractory infection of H. pylori group
The proportion of mix infection of H pylori in a total of 240 patients in two groups
The number of single nucleotide varation(SNV)of 20 patients in the first successful eradication group and the refractory infection of H. pylori group that are related to Amoxicillin resistance

Secondary Outcome Measures

Full Information

First Posted
March 25, 2016
Last Updated
July 10, 2016
Sponsor
Taizhou Hospital
Collaborators
Centers for Disease Control and Prevention, China, Academy Military Medical Science, China, First Affiliated Hospital of Zhejiang University, Taizhou Enze Medical Center (Group) Luqiao Hospital, Taizhou Enze Medical Center (Group) Enze Hospital, Taizhou First People's Hospital, The first people Hospital of Linhai, The first people Hospital of Wenling, Sanmen People Hospital, Xianju People Hospital, Tiantai People Hospital, Yuhuan People Hospital, The second people Hospital of Yuhuan, Zhiyuan Medical Inspection Institute
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1. Study Identification

Unique Protocol Identification Number
NCT02741414
Brief Title
A Multi-center Study for Eradication of Refractory Helicobacter Pylori
Official Title
Construction and Application of the Treatment of Refractory Helicobacter Pylori Infection Based on the High-throughput Sequencing Technologies
Study Type
Interventional

2. Study Status

Record Verification Date
March 2016
Overall Recruitment Status
Unknown status
Study Start Date
June 2016 (undefined)
Primary Completion Date
April 2018 (Anticipated)
Study Completion Date
December 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Taizhou Hospital
Collaborators
Centers for Disease Control and Prevention, China, Academy Military Medical Science, China, First Affiliated Hospital of Zhejiang University, Taizhou Enze Medical Center (Group) Luqiao Hospital, Taizhou Enze Medical Center (Group) Enze Hospital, Taizhou First People's Hospital, The first people Hospital of Linhai, The first people Hospital of Wenling, Sanmen People Hospital, Xianju People Hospital, Tiantai People Hospital, Yuhuan People Hospital, The second people Hospital of Yuhuan, Zhiyuan Medical Inspection Institute

4. Oversight

5. Study Description

Brief Summary
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastritis
Keywords
Helicobacter pylori, Antibiotic resistance, Sequencing, Mechanism

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
4428 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
H pylori culture negative group
Arm Type
Experimental
Arm Description
The patients who have the negative result of H pylori culture were classified into H pylori culture negative group.
Arm Title
The first successful eradication group
Arm Type
Experimental
Arm 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.
Arm Title
The refractory infection of H. pylori group
Arm Type
Experimental
Arm 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.
Intervention Type
Device
Intervention Name(s)
The result of H pylori culture based on gram staining and enzyme activity testing
Intervention Description
This intervention aimed at patients with the positive result of 13C-urea breath test. Patients with negative result of H pylori culture was H pylori culture negative group. Patients with positive result of H pylori culture were belonged into the first successful eradication group and the refractory infection of H. pylori group.
Intervention Type
Device
Intervention Name(s)
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
Intervention Description
The intervention focused on the results from the result of 13C-urea breath test after treatment. The first successful eradication group and the refractory infection of H. pylori group were treated according to the antibiotic susceptibility testing and CYP2C19 gene polymorphism. Eight weeks after treatment, a 13C-urea breath test was performed on patients. The first successful eradication group were patients with negative in 13C-urea breath tests in the first treatment. The refractory infection of H. pylori group were treatment failure patients with positive in 13C-urea breath tests after the second standardized treatment.
Intervention Type
Device
Intervention Name(s)
The result of Amoxicillin resistance in vitro based on antibiotic susceptibility testing
Intervention Description
The intervention focused on the results from the result of Amoxicillin susceptibility testing in vitro. In this study, the investigators selected the patients with Amoxicillin resistance from the first successful eradication group and the refractory infection of H. pylori group.
Primary Outcome Measure Information:
Title
The eradication rate of H. pylori reach to 95% in all groups
Time Frame
1 year
Title
The microflora structure of a total of 240 patients in the first successful eradication group and the refractory infection of H. pylori group
Time Frame
Three months
Title
The proportion of mix infection of H pylori in a total of 240 patients in two groups
Time Frame
Three months
Title
The number of single nucleotide varation(SNV)of 20 patients in the first successful eradication group and the refractory infection of H. pylori group that are related to Amoxicillin resistance
Time Frame
Three months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18~70 years old, male or female, the first eradication therapy of H. pylori infection patients. Symptoms of abdominal pain, bloating, acid efflux, belching, nausea, vomiting, heartburn, chest pain, vomiting, melena, etc. Unused antibiotics, bismuth, H2 receptor antagonists or PPIs by nearly 4 weeks 13C-labelled urea breath test positive. Agreed to Helicobacter pylori culture and sensitivity testing taken by endoscopy gastric biopsy specimens,and the result of culture was positive. Agreed to Helicobacter pylori eradication therapy and cooperate with the eradication efficacy follow-up survey. Exclusion Criteria: Severe heart, liver, kidney dysfunction. Pregnant or lactating women. Complications of bleeding, perforation, pyloric obstruction, cancer. Esophageal,gastrointestinal surgery history. Patients can not properly express their complaints,such as psychosis, severe neurosis. Taking nonsteroidal antiinflammatory drugs (NSAIDs) or alcohol abusers. Allergic to penicillin or either drugs of the 6 antibiotic tested by susceptibility testing.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Liping Ye, BSc
Phone
13566866269
Email
yelp@enzemed.com
Facility Information:
Facility Name
Xianju People Hospital
City
Taizhou
State/Province
Zhejiang
ZIP/Postal Code
317300
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hong Li Lyh
Phone
13586202668

12. IPD Sharing Statement

Learn more about this trial

A Multi-center Study for Eradication of Refractory Helicobacter Pylori

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