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Quadruple vs Tailored Therapy in the Treatment of Helicobacter Pylori Infection

Primary Purpose

Helicobacter Pylori Infection

Status
Completed
Phase
Not Applicable
Locations
Croatia
Study Type
Interventional
Intervention
Amoxicillin
Metronidazole
Clarithromycin
Pantoprazole 40mg
according to antibiogram
Sponsored by
University of Split, School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Helicobacter Pylori Infection

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • helicobacter pylori infection

Exclusion Criteria:

  • previous unsuccessful eradication treatment, stomach or other malignancy, taking of proton pump inhibitors, H2-antagonists, bismuth or antibiotics (amoxicillin, metronidazole, clarithromycin) in the previous month, significant comorbidities (renal insufficiency, psychiatric disease), denial to participate in the study, history of allergy to proton pump inhibitors or antibiotics, pregnancy and lactation.

Sites / Locations

  • University hospital Split

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

concomitant

tailored

Arm Description

Concomitant therapy consists of 14 days pantoprazole 40 mg, amoxicillin 1000 mg, clarithromycin 500 mg, metronidazole 500 mg all twice daily.

Tailored therapy consists of 14 days antibiotic therapy according to H. Pylori strains antibiotic sensitivity test together with pantoprazole 40 mg twice daily.

Outcomes

Primary Outcome Measures

eradication
H.pylori status will be tested 1 month after therapy with a stool antigen test: positive or negative

Secondary Outcome Measures

compliance
compliance will be measured by counting pills that were taken during therapy, more than or equal to 80% will be considered as good compliance
adverse event
patients will be asked to report any adverse events that occurred during treatment, they will be divided in groups, according to the degree of limitation of daily activities: no adverse events, mild (no limitations of activities), moderate (partially limited activities), severe (completely limited)

Full Information

First Posted
October 21, 2020
Last Updated
November 5, 2020
Sponsor
University of Split, School of Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT04621487
Brief Title
Quadruple vs Tailored Therapy in the Treatment of Helicobacter Pylori Infection
Official Title
A Randomized Controlled Trial: Quadruple vs Tailored Therapy in the Treatment of Helicobacter Pylori Infection
Study Type
Interventional

2. Study Status

Record Verification Date
October 2020
Overall Recruitment Status
Completed
Study Start Date
January 15, 2019 (Actual)
Primary Completion Date
January 15, 2020 (Actual)
Study Completion Date
February 15, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Split, School of Medicine

4. Oversight

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

5. Study Description

Brief Summary
Non-bismuth quadruple therapies have been proposed as potential strategies in improving the efficacy of first-line treatments. The non-bismuth quadruple therapy in its concomitant variant consists of proton pump inhibitor, amoxicillin, nitroimidazole and clarithromycin given concurrently twice daily. As a result of concurrent administration this therapy has given better results according to some studies in comparison to sequential variants. However, this therapy, as well suffers from the aforementioned increase in antibiotic resistance. Therefore, the aim of this study was to compare concomitant non-bismuth quadruple therapy with a tailored therapy based on antibiotic strain susceptibility testing.
Detailed Description
More than half of world population are H.pylori carriers. The infection is mostly acquired in childhood and persists lifelong. A notable risk factor is a lower social and economic status during childhood reflecting mostly poor hygienic standard or small and dense living area. Newly acquired infections in adulthood are a rarity. The reservoir of H. Pylori is the human stomach. H. pylori is considered to be the main pathogen involved in causing benign peptic ulcer and functional dyspepsia as well as gastric cancer. The treatment of H. Pylori infection is currently complicated by an increase in antimicrobial resistance in different parts of the world. Corresponding increase in clarithromycin as well as quinolone and metronidazole resistance poses a major clinical problem and calls for a new approach to treatment. Under such circumstances there is an emerging trend towards personalized eradication therapy. Since H. Pylori infection is an infectious disease its optimal treatment should both theoretically and practically be based on the specific characteristics of the strain and if possible the host of the infection. The aim of such an approach should be a better eradication efficacy. Non-bismuth quadruple therapies have been proposed as potential strategies in improving the efficacy of first-line treatments. The non-bismuth quadruple therapy in its concomitant variant consists of proton pump inhibitor, amoxicillin, nitroimidazole and clarithromycin given concurrently twice daily. As a result of concurrent administration this therapy has given better results according to some studies in comparison to sequential variants. However, this therapy, as well suffers from the aforementioned increase in antibiotic resistance. Therefore, the aim of this study was to compare concomitant non-bismuth quadruple therapy with a tailored therapy based on antibiotic strain susceptibility testing assuming that eradication rate with tailored therapy will be above 90%.

6. Conditions and Keywords

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

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
concomitant
Arm Type
Active Comparator
Arm Description
Concomitant therapy consists of 14 days pantoprazole 40 mg, amoxicillin 1000 mg, clarithromycin 500 mg, metronidazole 500 mg all twice daily.
Arm Title
tailored
Arm Type
Active Comparator
Arm Description
Tailored therapy consists of 14 days antibiotic therapy according to H. Pylori strains antibiotic sensitivity test together with pantoprazole 40 mg twice daily.
Intervention Type
Drug
Intervention Name(s)
Amoxicillin
Intervention Description
14 days 1 gr bid
Intervention Type
Drug
Intervention Name(s)
Metronidazole
Intervention Description
14 days 500 mg bid
Intervention Type
Drug
Intervention Name(s)
Clarithromycin
Intervention Description
14 days 500 mg bid
Intervention Type
Drug
Intervention Name(s)
Pantoprazole 40mg
Other Intervention Name(s)
Pantoprazole
Intervention Description
40 mg bid 14 days
Intervention Type
Drug
Intervention Name(s)
according to antibiogram
Intervention Description
according to antibiogram
Primary Outcome Measure Information:
Title
eradication
Description
H.pylori status will be tested 1 month after therapy with a stool antigen test: positive or negative
Time Frame
1 month after finishing therapy
Secondary Outcome Measure Information:
Title
compliance
Description
compliance will be measured by counting pills that were taken during therapy, more than or equal to 80% will be considered as good compliance
Time Frame
1 month after finishing therapy
Title
adverse event
Description
patients will be asked to report any adverse events that occurred during treatment, they will be divided in groups, according to the degree of limitation of daily activities: no adverse events, mild (no limitations of activities), moderate (partially limited activities), severe (completely limited)
Time Frame
1 month after finishing therapy

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: helicobacter pylori infection Exclusion Criteria: previous unsuccessful eradication treatment, stomach or other malignancy, taking of proton pump inhibitors, H2-antagonists, bismuth or antibiotics (amoxicillin, metronidazole, clarithromycin) in the previous month, significant comorbidities (renal insufficiency, psychiatric disease), denial to participate in the study, history of allergy to proton pump inhibitors or antibiotics, pregnancy and lactation.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nikola Perkovic, MD
Organizational Affiliation
University hospital Split
Official's Role
Principal Investigator
Facility Information:
Facility Name
University hospital Split
City
Split
ZIP/Postal Code
21000
Country
Croatia

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Quadruple vs Tailored Therapy in the Treatment of Helicobacter Pylori Infection

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