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A Comparison of Four Different Treatment Regimens of Helicobacter Pylori in Chinese Children

Primary Purpose

Helicobacter Infections

Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
triple therapy
sequential therapy
bismuth quadruple therapy
concomitant therapy
Sponsored by
Ying HUANG
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Helicobacter Infections

Eligibility Criteria

6 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • children 6-18 years of age who were referred for upper endoscopy and confirmed to have Hp infection

Exclusion Criteria:

  • patients were excluded if they had taken proton pump inhibitors, H2-receptor antagonists or antibiotics in the 4 weeks prior to the study. Patients with known antibiotic allergy,hepatic impairment or kidney failure were also excluded. Patients who received Hp therapy before were also excluded.

Sites / Locations

  • Children's hospital of Fudan universityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

T-group

S-group

B-group

C-group

Arm Description

T-group(triple therapy)

S-group( sequential therapy)

B-group( bismuth quadruple therapy )

C-group( concomitant therapy)

Outcomes

Primary Outcome Measures

13C-UBT
13C-UBT was used to determine whether Hp treatments was successful

Secondary Outcome Measures

side effects
such as diarrea,rash,dark stool
changes of Shannon diversity indices for gut microbiome
changes of the Shannon diversity indices
changes of OTU for gut microbiome
changes of OTU
changes of abundances for gut microbiome
changes of abundances of the bacteria
CYP2C19 gene that impact the metabolism of PPI
CYP2C19 gene polymorphism
virulence gene-cagA
cagA
virulence gene-vacA
vacA
patient compliance
good compliance is defined as taking more than 80% drugs

Full Information

First Posted
November 20, 2017
Last Updated
December 8, 2022
Sponsor
Ying HUANG
Collaborators
Guangzhou Women and Children's Medical Center, The Children's Hospital of Zhejiang University School of Medicine, Beijing Children's Hospital, Tang-Du Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03365609
Brief Title
A Comparison of Four Different Treatment Regimens of Helicobacter Pylori in Chinese Children
Official Title
A Comparison of Four Different Treatment Regimens as the First-line Treatment of Helicobacter Pylori in Chinese Children and Investigation of Resistance and Impact factors-a Multicenter Study
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 20, 2017 (Actual)
Primary Completion Date
October 1, 2025 (Anticipated)
Study Completion Date
December 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Ying HUANG
Collaborators
Guangzhou Women and Children's Medical Center, The Children's Hospital of Zhejiang University School of Medicine, Beijing Children's Hospital, Tang-Du Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
With the resistance of Helicobacter pylori increasing, low and unsatisfactory eradication rate (64%) have been observed with standard triple therapy in European children. Which regimen is appropriate for Chinese children? There is no large scale, multi center studies in China about treatment, CYP2C19 gene polymorphism, resistance rate and resistance genotype. Investigators want to perform a research to compare four different treatment regimens(triple therapy, sequential therapy, bismuth quadruple therapy and concomitant therapy)as the first-line treatment of Helicobacter pylori in Chinese children and investigation of resistance, impact factors and changes of microbiota after the therapy. The results of the study will provide theoretical basis to make the new guideline of diagnosis and therapy of Helicobacter pylori in Chinese children. It advance instruct and norm the clinical practice for Chinese pediatrician to increase the cure rate of Helicobacter pylori and decrease the resistance.
Detailed Description
Eligible children were randomly divided into four groups: standard triple therapy, sequential therapy, bismuth quadruple therapy and concomitant therapy. The course of treatment is 14 days. The primary outcome measure was the Hp eradication rate at 4-6 weeks after completion of treatment which was confirmed by a negative of 13 UBT. Secondary outcome measures included side effects, impact factor and changes of microbiome after the therapy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Helicobacter Infections

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1440 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
T-group
Arm Type
Experimental
Arm Description
T-group(triple therapy)
Arm Title
S-group
Arm Type
Experimental
Arm Description
S-group( sequential therapy)
Arm Title
B-group
Arm Type
Experimental
Arm Description
B-group( bismuth quadruple therapy )
Arm Title
C-group
Arm Type
Experimental
Arm Description
C-group( concomitant therapy)
Intervention Type
Drug
Intervention Name(s)
triple therapy
Intervention Description
Omeprazole+Amoxicillin+Clarithromycin
Intervention Type
Drug
Intervention Name(s)
sequential therapy
Intervention Description
the first 7 days : Omeprazole+Amoxicillin, the last 7 days: Omeprazole+Clarithromycin+Metronidazole
Intervention Type
Drug
Intervention Name(s)
bismuth quadruple therapy
Intervention Description
Omeprazole+Amoxicillin+Metronidazole+Colloidal Bismuth Subcitrate
Intervention Type
Drug
Intervention Name(s)
concomitant therapy
Intervention Description
Omeprazole+Amoxicillin+Clarithromycin+Metronidazole
Primary Outcome Measure Information:
Title
13C-UBT
Description
13C-UBT was used to determine whether Hp treatments was successful
Time Frame
13C-UBT was assessed at 4-6 weeks after completion of therapy
Secondary Outcome Measure Information:
Title
side effects
Description
such as diarrea,rash,dark stool
Time Frame
assess at 2,4-6weeks after completion of the therapy
Title
changes of Shannon diversity indices for gut microbiome
Description
changes of the Shannon diversity indices
Time Frame
assess at 0,2,4-6weeks after completion of the therapy
Title
changes of OTU for gut microbiome
Description
changes of OTU
Time Frame
assess at 0,2,4-6weeks after completion of the therapy
Title
changes of abundances for gut microbiome
Description
changes of abundances of the bacteria
Time Frame
assess at ,2,4-6weeks after completion of the therapy
Title
CYP2C19 gene that impact the metabolism of PPI
Description
CYP2C19 gene polymorphism
Time Frame
detect the gene before the therapy
Title
virulence gene-cagA
Description
cagA
Time Frame
detect the gene before the therapy
Title
virulence gene-vacA
Description
vacA
Time Frame
detect the gene before the therapy
Title
patient compliance
Description
good compliance is defined as taking more than 80% drugs
Time Frame
assess compliance 2 weeks after the therapy

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: children 6-18 years of age who were referred for upper endoscopy and confirmed to have Hp infection Exclusion Criteria: patients were excluded if they had taken proton pump inhibitors, H2-receptor antagonists or antibiotics in the 4 weeks prior to the study. Patients with known antibiotic allergy,hepatic impairment or kidney failure were also excluded. Patients who received Hp therapy before were also excluded.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ying Zhou, master
Phone
13917394900
Email
nnyyhhs@163.com
Facility Information:
Facility Name
Children's hospital of Fudan university
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
201102
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ying Huang, MD and PhD
Phone
13816882247
Email
yhuang815@163.com
First Name & Middle Initial & Last Name & Degree
Ying Zhou

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
28541262
Citation
Jones NL, Koletzko S, Goodman K, Bontems P, Cadranel S, Casswall T, Czinn S, Gold BD, Guarner J, Elitsur Y, Homan M, Kalach N, Kori M, Madrazo A, Megraud F, Papadopoulou A, Rowland M; ESPGHAN, NASPGHAN. Joint ESPGHAN/NASPGHAN Guidelines for the Management of Helicobacter pylori in Children and Adolescents (Update 2016). J Pediatr Gastroenterol Nutr. 2017 Jun;64(6):991-1003. doi: 10.1097/MPG.0000000000001594.
Results Reference
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A Comparison of Four Different Treatment Regimens of Helicobacter Pylori in Chinese Children

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