Increased Re-eradication Rate of Helicobacter Pylori by Adding N-acetylcystein or Metronidazole to the Triple Therapy
Primary Purpose
Bacterial Infection Due to Helicobacter Pylori (H. Pylori)
Status
Unknown status
Phase
Phase 4
Locations
Taiwan
Study Type
Interventional
Intervention
10RAC+acetylcystein
10RAC+metronidazole
Sponsored by
About this trial
This is an interventional treatment trial for Bacterial Infection Due to Helicobacter Pylori (H. Pylori) focused on measuring Helicobacter pylori, antibiotic resistance, N-acetylcystein, biofilm, second-line eradication treatment
Eligibility Criteria
Inclusion Criteria:
- Patient after treatment for Helicobacter pylori eradication.
- Still clinically with evidence of gastric Helicobacter pylori infection.
Exclusion Criteria:
- woman in breast feeding or pregnancy.
- allergy to drugs used in study.
- never treated for H. pylori.
- intolerance to fructose, lactose.
- patients with hematologic, brain or spinal disorders.
- patients under 20 years old.
- patients with malignancy or with decompensated function of vital organs.
Sites / Locations
- Buddhist Tzu Chi General HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Acetylcystein
Metronidazole
Arm Description
10-day triple therapy plus N-acetyl-cystein to remove the biofilm.
10-day triple therapy plus metronidazole (concomitant therapy) as active comparator
Outcomes
Primary Outcome Measures
Re-eradication rate
A negative post-treatment 13C-urea breath test result at more than 4 weeks after complete use of drug for treatment.
Secondary Outcome Measures
Influence of Participant's CYP2C19 genotype on re-eradication rate
Influence of Participant's CYP2C19 genotype (EM, IM or PM) on re-eradication rate of Helicobacter pylori
Full Information
NCT ID
NCT01572597
First Posted
April 4, 2012
Last Updated
April 5, 2012
Sponsor
Buddhist Tzu Chi General Hospital
1. Study Identification
Unique Protocol Identification Number
NCT01572597
Brief Title
Increased Re-eradication Rate of Helicobacter Pylori by Adding N-acetylcystein or Metronidazole to the Triple Therapy
Official Title
Increased Second-line Eradication Rate of Helicobacter Pylori by Adding N-acetylcystein or Metronidazole to the Conventional Triple Therapy.
Study Type
Interventional
2. Study Status
Record Verification Date
April 2012
Overall Recruitment Status
Unknown status
Study Start Date
June 2011 (undefined)
Primary Completion Date
December 2012 (Anticipated)
Study Completion Date
December 2012 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Buddhist Tzu Chi General Hospital
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Compare efficacy and safety of 10-day triple therapy (rabeprazole, clarithromycin and amoxicillin) plus N-acetylcystein versus 10-day concomitant therapy (rabeprazole, clarithromycin, amoxicillin and metronidazole) for re-eradication for gastric Helicobacter pylori infection.
Detailed Description
Background: Antimicrobial resistance has decreased the eradication rates of common used triple therapy for Helicobacter pylori infection (less than 80%). Such treatment for patient previously with treatment failure, the retreatment eradication rate is less then 50%. Some studies showed the Helicobacter pylori form biofilm to prevent entry of antibiotics, and the N-acetylcystein is helpful to dissolve the biofilm.
Objective: To determine the eradication rate of the common used triple therapy after adding N-acetylcystein for second line treatment for adults infected with Helicobacter pylori in Eastern Taiwan.
Design: Randomized, open-label, prospective controlled trial.
Patients: who are previously failed the primary treatment for eradication and still infected by Helicobacter pylori.
Measurements: 13C-urea breath test, upper endoscopy, histologic evaluation, rapid urease test, bacterial culture, assessment of antibiotic resistance and CYP2C19 genotype of host.
Intervention: patients with Helicobacter pylori eradication treatment failure are recruited and randomly assigned to receive one of the following therapeutic schemes: 1) study group: rabeprazole 20mg bid + amoxicillin 1g bid + clarithromycin 0.5g bid + N-acetylcystein 0.6g bid for 10 days; 2) control group: rabeprazole 20mg bid + amoxicillin 1g bid + clarithromycin 0.5g bid + metronidazole 0.5g bid for 10 days. Repeat upper endoscopy for histologic evaluation, rapid urease test or 13C-urea breath test after 4 week of treatment to assess the treatment result. The influence on the hybrid therapies of antibiotic resistance of Helicobacter pylori and CYP2C19 genotype of host were determined.
Expected results: The new second line treatment for eradication of Helicobacter pylori is effective, and to determine the relation of antibiotic resistance of Helicobacter pylori and CYP2C19 genotype of host to the treatment result.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bacterial Infection Due to Helicobacter Pylori (H. Pylori)
Keywords
Helicobacter pylori, antibiotic resistance, N-acetylcystein, biofilm, second-line eradication treatment
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Acetylcystein
Arm Type
Experimental
Arm Description
10-day triple therapy plus N-acetyl-cystein to remove the biofilm.
Arm Title
Metronidazole
Arm Type
Active Comparator
Arm Description
10-day triple therapy plus metronidazole (concomitant therapy) as active comparator
Intervention Type
Drug
Intervention Name(s)
10RAC+acetylcystein
Other Intervention Name(s)
Pariet, Klaricid, Hiconcil, Fluimucil
Intervention Description
10-days rabeprazole 20mg b.i.d + clarithromycin 500mg b.i.d + amoxicillin 1000mg b.i.d + N-acetyl-cystein 600mg b.i.d
Intervention Type
Drug
Intervention Name(s)
10RAC+metronidazole
Other Intervention Name(s)
Pariet, Klaricid, Hiconcil, Flagyl
Intervention Description
10-days rabeprazole 20mg b.i.d + clarithromycin 500mg b.i.d + amoxicillin 1000mg b.i.d + metronidazole 500mg b.i.d
Primary Outcome Measure Information:
Title
Re-eradication rate
Description
A negative post-treatment 13C-urea breath test result at more than 4 weeks after complete use of drug for treatment.
Time Frame
4 weeks after complete use of drug for treatment
Secondary Outcome Measure Information:
Title
Influence of Participant's CYP2C19 genotype on re-eradication rate
Description
Influence of Participant's CYP2C19 genotype (EM, IM or PM) on re-eradication rate of Helicobacter pylori
Time Frame
4 weeks after complete use of drug for treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patient after treatment for Helicobacter pylori eradication.
Still clinically with evidence of gastric Helicobacter pylori infection.
Exclusion Criteria:
woman in breast feeding or pregnancy.
allergy to drugs used in study.
never treated for H. pylori.
intolerance to fructose, lactose.
patients with hematologic, brain or spinal disorders.
patients under 20 years old.
patients with malignancy or with decompensated function of vital organs.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ming-Cheh CHEN, M.D.
Phone
+886-910-521003
Email
MingCheh_chen@tzuchi.com.tw
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ming-Cheh CHEN, MD
Organizational Affiliation
Buddhist Tzu Chi General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Buddhist Tzu Chi General Hospital
City
Hualien
ZIP/Postal Code
97002
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ming-Cheh CHEN, MD
Phone
+886-910-521003
Email
MingCheh_chen@tzuchi.com.tw
First Name & Middle Initial & Last Name & Degree
Chi-Tan HU, PhD, MD
First Name & Middle Initial & Last Name & Degree
Wei-Yi RAY, MD
12. IPD Sharing Statement
Citations:
PubMed Identifier
19804842
Citation
Wu DC, Hsu PI, Wu JY, Opekun AR, Kuo CH, Wu IC, Wang SS, Chen A, Hung WC, Graham DY. Sequential and concomitant therapy with four drugs is equally effective for eradication of H pylori infection. Clin Gastroenterol Hepatol. 2010 Jan;8(1):36-41.e1. doi: 10.1016/j.cgh.2009.09.030. Epub 2009 Oct 3.
Results Reference
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PubMed Identifier
20478402
Citation
Cammarota G, Branca G, Ardito F, Sanguinetti M, Ianiro G, Cianci R, Torelli R, Masala G, Gasbarrini A, Fadda G, Landolfi R, Gasbarrini G. Biofilm demolition and antibiotic treatment to eradicate resistant Helicobacter pylori: a clinical trial. Clin Gastroenterol Hepatol. 2010 Sep;8(9):817-820.e3. doi: 10.1016/j.cgh.2010.05.006. Epub 2010 May 31.
Results Reference
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Increased Re-eradication Rate of Helicobacter Pylori by Adding N-acetylcystein or Metronidazole to the Triple Therapy
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