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High Dose PPI Triple Therapy Versus Sequential Therapy for Helicobacter Pylori Eradication

Primary Purpose

Dyspepsia, Helicobacter-associated Gastritis, Stomach Disorders

Status
Completed
Phase
Phase 4
Locations
Thailand
Study Type
Interventional
Intervention
Double dose of PPI
sequence of drug use
Sponsored by
Mahidol University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dyspepsia focused on measuring Dyspepsia, Helicobacter pylori, Clarithromycin resistance, Other Specified Disorders of Function of Stomach

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Functional dyspepsia patients (Rome III) with rapid urease test positive
  • Age ≥ 18 years old
  • No history of HP eradication

Exclusion Criteria:

  • Recent use of PPI, H2RA, NSAID, Antibiotics within 2 weeks
  • Currently use of anticoagulants or ketoconazole
  • C/I for gastric biopsy
  • History of gastric surgery
  • Comorbidity: ESRD, advanced cirrhosis, AIDS, stroke (bed ridden)
  • Pregnancy or lactation
  • Allergy to studied drugs

Sites / Locations

  • Division of gastroenterology, Department of Medicine, Siriraj hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Sequential therapy (ST)

High dose PPI triple therapy(TT)

Arm Description

10 day Sequential therapy: lansoprazole 30 mg b.d. plus amoxicillin 1000 mg b.d. for 5 days then lansoprazole 30 mg b.d., metronidazole 400 mg b.d. and clarithromycin 500 mg b.d. for the remaining 5 days

10 day high dose PPI triple therapy: lansoprazole 60 mg b.d. plus clarithromycin 500 mg b.d. and amoxycillin 1000 mg b.d. for 10 days

Outcomes

Primary Outcome Measures

Eradication rate

Secondary Outcome Measures

Adherence rate/adverse events
Prevalence of clarithromycin resistance HP
Symptomatic responses regarding dyspeptic symptoms after HP eradication

Full Information

First Posted
June 25, 2013
Last Updated
April 9, 2015
Sponsor
Mahidol University
Collaborators
Takeda Pharmaceuticals International, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT01888237
Brief Title
High Dose PPI Triple Therapy Versus Sequential Therapy for Helicobacter Pylori Eradication
Official Title
Randomized Open Labeled Clinical Trial: a Comparative Study of 10-day High Dose PPI-based Triple Therapy vs. 10-day Sequential Therapy for Helicobacter Pylori Eradication in Functional Dyspepsia Patients
Study Type
Interventional

2. Study Status

Record Verification Date
April 2015
Overall Recruitment Status
Completed
Study Start Date
May 2013 (undefined)
Primary Completion Date
August 2014 (Actual)
Study Completion Date
September 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mahidol University
Collaborators
Takeda Pharmaceuticals International, Inc.

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to compare the efficacy between 1-day high dose PPI-based triple therapy vs. 10-day sequential therapy for Helicobacter pylori eradication in functional dyspepsia patients.
Detailed Description
Background: Helicobacter pylori (HP) play an important role in the pathogenesis of chronic gastritis, peptic ulcer diseases as well as gastric cancer. Helicobacter pylori eradication is a critical strategy to reduce aforementioned conditions. Proton-pump inhibitor (PPI)-based triple therapy (Standard dose PPIs+ Clarithromycin 1g/D + Amoxycillin 2g/D or Metronidazole 800 mg/D) is recommended as a frontline treatment in current guidelines for HP eradication, both from Thai and Second Asia-Pacific Consensus Guideline for H.pylori 2009. Unfortunately, it has been reported an unacceptably low eradication rate (<85%) of this regimen in a tertiary care hospital in Thailand. This occurrence is not surprised as the worldwide efficacy of this regimen had decreased to 50-75%. Of this, Clarithromycin resistance has been a major cause of the treatment failure. Sequential therapy (ST) which consists of standard dose PPIs + amoxycillin 2 g/D for 5 days with 5 additional days of clarithromycin 1g/D + metronidazole 800 mg/D has been proposed to increase an efficacy in HP eradication. A recent meta-analysis of over three thousand population revealed a higher eradication rate over PPI-based triple therapy (TT). A consistent finding from Thailand was reported an impressive success rate of ST in HP eradication up to 95%. Therefore, more updated guidelines recommend using ST, not TT, as the first line regimen. However, ST is a complicated regimen for the patients to be followed. This might cause a low adherence rate in clinical practice as well as development of drug resistance in near future. Interestingly, PPI is a pivotal in all regimens in HP eradication. There is evidence that the sustained higher intragastric pH is a major therapeutic determinant of HP eradication. Other factors including inflammatory cytokine polymorphisms, especially the IL-1B-511 T/T genotype and PPIs metabolizer, are the determinants of eradication by affecting gastric acid secretion and mucosal inflammation. Hence, higher dosage of PPIs is justified to eradicate HP. This has been shown in a recent meta-analysis that high dose PPI is better than standard dose PPI triple therapy in HP eradication of HP. Our study aims to compare the efficacy of ST to high dose PPI TT. Secondary outcomes include comparisons in the adherence and adverse events between both regimens, to determine the prevalence of clarithromycin resistance HP and determine improvement of dyspeptic symptoms after HP eradication Primary Aim/Objective: To evaluate eradication rates of Helicobacter pylori infection in functional dyspepsia patients amongst Thai population, compare between a 10-day sequential regimen (lansoprazole 30 mg b.d. plus amoxicillin 1000 mg b.d. for 5 days then lansoprazole 30 mg b.d., metronidazole 400 mg b.d. and clarithromycin 500 mg b.d. for the remaining 5 days) with a 10-day high dose PPI-based triple regimen (lansoprazole 60 mg b.d. plus clarithromycin 500 mg b.d. and amoxycillin 1000 mg b.d. for 10 days)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dyspepsia, Helicobacter-associated Gastritis, Stomach Disorders
Keywords
Dyspepsia, Helicobacter pylori, Clarithromycin resistance, Other Specified Disorders of Function of Stomach

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
118 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Sequential therapy (ST)
Arm Type
Active Comparator
Arm Description
10 day Sequential therapy: lansoprazole 30 mg b.d. plus amoxicillin 1000 mg b.d. for 5 days then lansoprazole 30 mg b.d., metronidazole 400 mg b.d. and clarithromycin 500 mg b.d. for the remaining 5 days
Arm Title
High dose PPI triple therapy(TT)
Arm Type
Experimental
Arm Description
10 day high dose PPI triple therapy: lansoprazole 60 mg b.d. plus clarithromycin 500 mg b.d. and amoxycillin 1000 mg b.d. for 10 days
Intervention Type
Drug
Intervention Name(s)
Double dose of PPI
Intervention Description
Lansoprasole (30mg) 2 tab oral BID
Intervention Type
Drug
Intervention Name(s)
sequence of drug use
Intervention Description
lansoprazole 30 mg b.d. for 10 days amoxicillin 1000 mg b.d. (day 1 to day 5) metronidazole 400 mg b.d. (day 6-day 10) and clarithromycin 500 mg b.d. (day 6-day 10)
Primary Outcome Measure Information:
Title
Eradication rate
Time Frame
4 weeks after the end of intervention
Secondary Outcome Measure Information:
Title
Adherence rate/adverse events
Time Frame
up to 2 weeks after intervention initiation
Title
Prevalence of clarithromycin resistance HP
Time Frame
4 weeks after the end of intervention
Title
Symptomatic responses regarding dyspeptic symptoms after HP eradication
Time Frame
Baseline, week 4,8 and 24 after intervention completion

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Functional dyspepsia patients (Rome III) with rapid urease test positive Age ≥ 18 years old No history of HP eradication Exclusion Criteria: Recent use of PPI, H2RA, NSAID, Antibiotics within 2 weeks Currently use of anticoagulants or ketoconazole C/I for gastric biopsy History of gastric surgery Comorbidity: ESRD, advanced cirrhosis, AIDS, stroke (bed ridden) Pregnancy or lactation Allergy to studied drugs
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
monthira maneerattanaporn
Organizational Affiliation
Division of gastroenterology, Department of Medicine, Siriraj hospital 2, Pran-nok, Bangkoknoi, Bangkok, Thailand, Mahidol University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Division of gastroenterology, Department of Medicine, Siriraj hospital
City
Bangkok Noi
State/Province
Bangkok,
ZIP/Postal Code
10700
Country
Thailand

12. IPD Sharing Statement

Citations:
PubMed Identifier
29804294
Citation
Auesomwang C, Maneerattanaporn M, Chey WD, Kiratisin P, Leelakusolwong S, Tanwandee T. Ten-day high-dose proton pump inhibitor triple therapy versus sequential therapy for Helicobacter pylori eradication. J Gastroenterol Hepatol. 2018 Nov;33(11):1822-1828. doi: 10.1111/jgh.14292. Epub 2018 Jun 27.
Results Reference
derived

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High Dose PPI Triple Therapy Versus Sequential Therapy for Helicobacter Pylori Eradication

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