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Comparison of Sequential or Concomitant Therapy for Helicobacter Pylori Infection (960025)

Primary Purpose

Helicobacter Infection

Status
Completed
Phase
Phase 4
Locations
Taiwan
Study Type
Interventional
Intervention
10-day sequential treatment
10-day concomitant therapy
Sponsored by
Kaohsiung Veterans General Hospital.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Helicobacter Infection focused on measuring peptic ulcer disease, gastric cancer, therapeutics

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Male or non-pregnant female aged 18 to 75 years inclusively.
  • Mental and legal ability to give a written informed consent.
  • Active H. pylori infection.

Exclusion Criteria:

  • Previous surgery of the stomach such as partial gastrectomy.
  • Use of antibiotics within the preceding 30 days.
  • Regular use of bismuth compounds (>3 times per week) in the 30 days before enrollment.
  • Presence of serious medical condition(s) precluding participation or endoscopy with biopsy.
  • Use of concomitant medication(s) known to interact with study medication.
  • Presence of Zollinger-Ellison Syndrome.
  • Pregnancy or lactation.
  • Allergy to any of the study medications.
  • Contraindication(s) to the use of any of the study drugs.
  • Participation in a clinical trial within the last 30 days.
  • Unwillingness to abstain from alcoholic beverages.
  • Patients taking other medications including warfarin, antipsychotics, or chronic NSAIDs will also be excluded. Aspirin at a dose not more than 325 mg/day will be permitted.

Sites / Locations

  • Chung-Ho Hospital
  • Kaohsiung Veterans General Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

10-day concomitant therapy

10-day sequential therapy

Arm Description

esomeprazole and amoxicillin and clarithromycin and metronidazole for 10 days

esomeprazole and amoxicillin for 5 days, followed by esoprazole and clarithromycin and metronidazole for 5 more days

Outcomes

Primary Outcome Measures

Number of Participants in Which H. Pylori Was Eradicated
Evaluate eradication outcome by endoscopy urease test and histology or urea breath test
Number of Participants Who Had Good Drug Compliance
Good drug compliance is defined as taking equal to or more than 80% of eradication medicines

Secondary Outcome Measures

Full Information

First Posted
January 3, 2008
Last Updated
September 14, 2015
Sponsor
Kaohsiung Veterans General Hospital.
Collaborators
Baylor College of Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT00656968
Brief Title
Comparison of Sequential or Concomitant Therapy for Helicobacter Pylori Infection
Acronym
960025
Official Title
Sequential Versus Concomitant Therapy for Helicobacter Pylori Infection
Study Type
Interventional

2. Study Status

Record Verification Date
September 2015
Overall Recruitment Status
Completed
Study Start Date
May 2007 (undefined)
Primary Completion Date
June 2010 (Actual)
Study Completion Date
June 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Kaohsiung Veterans General Hospital.
Collaborators
Baylor College of Medicine

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Helicobacter pylori is a bacteria that infects the lining of the stomach and is associated with ulcers. Helicobacter pylori may also increase the long-term risk of developing certain forms of gastric cancer. Curing this infection generally requires that patients take 2 or more antibiotic medications and a stomach acid suppressing medication for about two weeks. Current treatments do not always cure the infection and a new treatment is being tested in this study. The drugs involved in the new 4 drug treatment have been widely used for treatment of this infection. It remains unknown what is the best and most cost effective way to give them. This study will compare three different ways of using these drugs. Subjects must have active Helicobacter pylori infection in order to participate in this study.
Detailed Description
The purpose of this study is to compare different methods of giving combination drug therapy for treating Helicobacter pylori infection of the stomach. The entire study will last less than 2 years. Each subject will be participating in the study for approximately 60 days. A total of 360 subjects will be asked to participate in this study. Before participating in this study, subject's must have undergone to confirm the presence and to assess the susceptibility of Helicobacter pylori. Qualified subjects will receive 4 drugs which are to be taken as part of the study treatment: an acid suppressing drug (name), amoxicillin, clarithromycin and metronidazole. The doses are 1 grams of amoxicillin, 40 mg of esomeprazole (Nexium), 500 mg of metronidazole and 250 mg of clarithromycin. Each drug will be given twice a day to be taken twice a day with the morning and evening meals. Subjects will receive one of three different combinations. The choice of which will be randomly chosen by the use of a computer program. The regimes are: all 4 drugs daily for 5 days, all 4 drugs daily for 10 days, and two drugs (esomeprazole and amoxicillin) for 5 days then all for drugs for 5 additional days. Subjects will be asked to return within 4 days after completion of the treatment to evaluate how they did with the drugs. They will be asked bring back all unused medication and the bottles or containers that the medicine was packaged in. Your medication use and tolerance to the study drugs will be assessed. The treatment portion of the study will be complete at this point. Evaluation of the effect of the treatment will take place 4-6 weeks after the end of therapy. Subjects will come back to the study site and will have a UBT or repeat endoscopy, if clinically indicated to verify that the Helicobacter pylori has been cured. Subjects will be asked not to take antibiotics or any other drugs that may affect the outcome of the breath test used to confirm that the treatment was successful.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Helicobacter Infection
Keywords
peptic ulcer disease, gastric cancer, therapeutics

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
232 (Actual)

8. Arms, Groups, and Interventions

Arm Title
10-day concomitant therapy
Arm Type
Active Comparator
Arm Description
esomeprazole and amoxicillin and clarithromycin and metronidazole for 10 days
Arm Title
10-day sequential therapy
Arm Type
Experimental
Arm Description
esomeprazole and amoxicillin for 5 days, followed by esoprazole and clarithromycin and metronidazole for 5 more days
Intervention Type
Drug
Intervention Name(s)
10-day sequential treatment
Other Intervention Name(s)
Nexium-based sequential therapy
Intervention Description
esomeprazole (40 mg daily) from day 1 to day 10, amoxicillin (1 g, bid) from day 1 to day 5, clarithromycin (500 mg, bid) from day 6 to day 10, metronidazole (500 mg, bid) from day 6 to day 10
Intervention Type
Drug
Intervention Name(s)
10-day concomitant therapy
Other Intervention Name(s)
Nexium-based quadruple therapy
Intervention Description
esomeprazole (40 mg, bid) from day 1 to day 10, amoxicillin (1 g, bid) from day 1 to day 10, clarithromycin (500 mg, bid) from day 1 to day 10, metronidazole (500 mg, bid) from day 1 to day 10
Primary Outcome Measure Information:
Title
Number of Participants in Which H. Pylori Was Eradicated
Description
Evaluate eradication outcome by endoscopy urease test and histology or urea breath test
Time Frame
one month after finishing study drugs
Title
Number of Participants Who Had Good Drug Compliance
Description
Good drug compliance is defined as taking equal to or more than 80% of eradication medicines
Time Frame
one month after finishing test therapy

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or non-pregnant female aged 18 to 75 years inclusively. Mental and legal ability to give a written informed consent. Active H. pylori infection. Exclusion Criteria: Previous surgery of the stomach such as partial gastrectomy. Use of antibiotics within the preceding 30 days. Regular use of bismuth compounds (>3 times per week) in the 30 days before enrollment. Presence of serious medical condition(s) precluding participation or endoscopy with biopsy. Use of concomitant medication(s) known to interact with study medication. Presence of Zollinger-Ellison Syndrome. Pregnancy or lactation. Allergy to any of the study medications. Contraindication(s) to the use of any of the study drugs. Participation in a clinical trial within the last 30 days. Unwillingness to abstain from alcoholic beverages. Patients taking other medications including warfarin, antipsychotics, or chronic NSAIDs will also be excluded. Aspirin at a dose not more than 325 mg/day will be permitted.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ching-Kuan Liu, MD, PhD
Organizational Affiliation
Kaohsiung Medical Univestity
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
David Y Graham, MD
Organizational Affiliation
Baylor College of Medicine
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Antone R Opekun, PA-C
Organizational Affiliation
Baylor College of Medicine
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Deng-Chyang Wu, MD PhD
Organizational Affiliation
Kaohsiung Medical University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Chung-Ho Hospital
City
Kaohsiung
ZIP/Postal Code
807
Country
Taiwan
Facility Name
Kaohsiung Veterans General Hospital
City
Kaohsiung
ZIP/Postal Code
813
Country
Taiwan

12. IPD Sharing Statement

Citations:
PubMed Identifier
16285942
Citation
Francavilla R, Lionetti E, Castellaneta SP, Magista AM, Boscarelli G, Piscitelli D, Amoruso A, Di Leo A, Miniello VL, Francavilla A, Cavallo L, Ierardi E. Improved efficacy of 10-Day sequential treatment for Helicobacter pylori eradication in children: a randomized trial. Gastroenterology. 2005 Nov;129(5):1414-9. doi: 10.1053/j.gastro.2005.09.007.
Results Reference
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Comparison of Sequential or Concomitant Therapy for Helicobacter Pylori Infection

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