Efficacy on Helicobacter Pylori Eradication With Two Antibiotic Regimens
Primary Purpose
Helicobacter Infections
Status
Completed
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Sequential therapy
Triple therapy
Sponsored by
About this trial
This is an interventional treatment trial for Helicobacter Infections focused on measuring Sequential therapy, Triple therapy, Eradication
Eligibility Criteria
Inclusion Criteria:
- Helicobacter pylori infection in biopsy
- Eradication required
Exclusion Criteria:
- Antibiotic received two weeks prior
- Previous treatment for H pylori infection
- Allergy to any of the treatment drugs
- Smoking > 5 cigarettes daily.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Sequential therapy
Triple therapy
Arm Description
Patient receive Omeprazole plus amoxicillin during 5 days and then omeprazole plus clarithromycin and metronidazole during another 5 days
Patient receive Omeprazole plus clarithromycin and amoxicillin during 14 days
Outcomes
Primary Outcome Measures
Eradication
Helicobacter pylori in gastric biopsy
Secondary Outcome Measures
Side effects
Nausea, vomiting, stomach ache
Full Information
NCT ID
NCT02395458
First Posted
March 12, 2015
Last Updated
March 17, 2015
Sponsor
Coordinación de Investigación en Salud, Mexico
1. Study Identification
Unique Protocol Identification Number
NCT02395458
Brief Title
Efficacy on Helicobacter Pylori Eradication With Two Antibiotic Regimens
Official Title
Efficacy on Helicobacter Pylori Eradication With Sequential Antibiotic Compared to Triple Therapy for 14 Days
Study Type
Interventional
2. Study Status
Record Verification Date
March 2015
Overall Recruitment Status
Completed
Study Start Date
March 2013 (undefined)
Primary Completion Date
February 2015 (Actual)
Study Completion Date
February 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Coordinación de Investigación en Salud, Mexico
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Clinical trial to compare efficacy on eradicating Helicobacter pylori with two antibiotic strategies: sequential with amoxicillin and omeprazole 5 days and clarithromycin with metronidazole and omeprazole 5 days or omeprazole with clarithromycin and amoxicillin 14 days.
Detailed Description
In patients with documented infection with Helicobacter pylori after endoscopy and biopsy, two modalities of treatment were compared, and after a control endoscopy and biopsy, eradication was assessed as well as side effects of both treatments.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Helicobacter Infections
Keywords
Sequential therapy, Triple therapy, Eradication
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
142 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Sequential therapy
Arm Type
Experimental
Arm Description
Patient receive Omeprazole plus amoxicillin during 5 days and then omeprazole plus clarithromycin and metronidazole during another 5 days
Arm Title
Triple therapy
Arm Type
Active Comparator
Arm Description
Patient receive Omeprazole plus clarithromycin and amoxicillin during 14 days
Intervention Type
Drug
Intervention Name(s)
Sequential therapy
Other Intervention Name(s)
Omeprazole-Amoxicillin-Clarithromycin-Metronidazole
Intervention Description
Patient receive Omeprazole plus amoxicillin during 5 days and then omeprazole plus clarithromycin and metronidazole during another 5 days
Intervention Type
Drug
Intervention Name(s)
Triple therapy
Other Intervention Name(s)
Omeprazole-Clarithromycin-Metronidazole
Intervention Description
Patient receive Omeprazole plus amoxicillin and Clarithromycin during 14 days
Primary Outcome Measure Information:
Title
Eradication
Description
Helicobacter pylori in gastric biopsy
Time Frame
6 to 8 week after treatment
Secondary Outcome Measure Information:
Title
Side effects
Description
Nausea, vomiting, stomach ache
Time Frame
two weeks after beginning of treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Helicobacter pylori infection in biopsy
Eradication required
Exclusion Criteria:
Antibiotic received two weeks prior
Previous treatment for H pylori infection
Allergy to any of the treatment drugs
Smoking > 5 cigarettes daily.
12. IPD Sharing Statement
Learn more about this trial
Efficacy on Helicobacter Pylori Eradication With Two Antibiotic Regimens
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