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Comparison Between Quadruple Regimens for Helicobacter Pylori Infection in Egypt

Primary Purpose

Helicobacter Pylori Infection

Status
Completed
Phase
Phase 4
Locations
Egypt
Study Type
Interventional
Intervention
Hybrid regimen
Reverse hybrid regimen
Levofloxacin quadruple regimen
Sponsored by
Ayman Magd Eldin Mohammad Sadek
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Helicobacter Pylori Infection focused on measuring Helicobacter Pylori Infection, Quadruple Therapy, Egypt

Eligibility Criteria

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

Inclusion Criteria:

  • Positive Helicobacter pylori antigen in the stool
  • Treatment-naive

Exclusion Criteria:

  • Previous treatment for Helicobacter pylori
  • Drug hypersensitivity

Sites / Locations

  • Faculty of Human Medicine, Zagazig University

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Active Comparator

Arm Label

(1) Hybrid regimen

(2) Reverse hybrid regimen

(3) Levofloxacin quadruple regimen

Arm Description

omeprazole 20mg bid, and amoxicillin 1gm bid in the 1st week, then clarithromycin 500mg bid, omeprazole 20mg bid, amoxicillin 1gm bid, and metronidazole 500mg tid in the 2nd week.

clarithromycin 500mg bid, omeprazole 20mg bid, amoxicillin 1gm bid, and metronidazole 500mg tid for 1 week, followed by omeprazole 20mg bid, and amoxicillin 1gm bid in the 2nd week.

levofloxacin 250mg QD, omeprazole 40mg QD, nitazoxanide 500mg bid, and doxycycline 100mg QD for 10 days. (LOAD)

Outcomes

Primary Outcome Measures

Percentage of Helicobacter Pylori Infection Cure
Measuring the curative rate of each regimen by a fecal antigen test
Incidence of Treatment-Emergent Adverse Events
Questionnaire to measure the number of Participants with Treatment-Emergent Adverse Events

Secondary Outcome Measures

Rate of Helicobacter Pylori Treatment Completion
Questionnaire to evaluate the compliance with each treatment regimen

Full Information

First Posted
July 4, 2019
Last Updated
November 23, 2019
Sponsor
Ayman Magd Eldin Mohammad Sadek
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1. Study Identification

Unique Protocol Identification Number
NCT04039412
Brief Title
Comparison Between Quadruple Regimens for Helicobacter Pylori Infection in Egypt
Official Title
Comparison Between Hybrid, Reverse Hybrid, and Non-Bismuth Levofloxacin Quadruple Regimens for Helicobacter Pylori Infection in Egypt: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2019
Overall Recruitment Status
Completed
Study Start Date
June 1, 2018 (Actual)
Primary Completion Date
December 22, 2018 (Actual)
Study Completion Date
June 30, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Ayman Magd Eldin Mohammad Sadek

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
The overall prevalence of H. Pylori in the developing countries is 50.8%, with the highest one presented in Africa (79.1%). Hybrid therapy is supposed to be more effective as a first-line regimen for Helicobacter pylori infection in Egypt than the Reverse hybrid and non-bismuth Levofloxacin quadruple therapies. We are aiming here to compare the Hybrid, Reverse hybrid, and Levofloxacin quadruple therapies as first-line therapy, trying to reach the safest, cost-effective, and compliance-inducing regimen in Egypt. We will conduct a randomized controlled (interventional) study at Zagazig University Hospital, internal medicine department clinic, on 330 patients. 110 patients will be allocated to each regimen.
Detailed Description
Introduction: Although the decreasing prevalence of Helicobacter Pylori (H. Pylori) worldwide, it remains high in developing countries. According to the most recent studies, the overall prevalence of H. Pylori in the developing countries is 50.8%, with the highest one presented in Africa (79.1%). Unfortunately, the data on the prevalence of H. Pylori, are not available from all the countries of Africa. There is a paucity of information about the magnitude of the problem in Egypt, according to the few available studies, the prevalence is ranging from 71.7-91.7%. The importance of H. Pylori infection lies in the major role in chronic gastritis, gastric ulcer, and duodenal ulcer, up to gastric adenocarcinoma, and gastric mucosa-associated lymphoid tissue lymphoma. Diagnosis of H. Pylori can be through invasive tests, which are cumbersome and expensive despite their high sensitivity and specificity. On the contrary, there are more easily and cheaper non-invasive tests, especially H. Pylori stool antigen and urea breath test that has a higher sensitivity than serology. The decreasing eradication rate of the standard triple therapy (STT) below 80% due to the emergence of resistant strains to Clarithromycin, raise the need for newer therapies that provide higher efficacy, and in the same time, better safety and compliance. Bismuth-containing quadruple therapy came as the treatment of choice that avoids Clarithromycin use, but it was a non-reasonable option for the countries that are lacking in bismuth salts and/or tetracycline, beside of the complex administration and low safety. It raises the era of the competing sequential and concomitant non-bismuth (clarithromycin containing) quadruple treatments. A novel two-step (dual-quadruple) treatment called the hybrid therapy (HT), which is actually a combined sequential and concomitant therapy, with a lower cost and better efficacy. However, the adding of two drugs in the last seven days of the therapy may confuse the patient, making him less willing to complete the treatment that promote the idea of reversing the sequence (quadruple-dual) in what is called the reverse hybrid therapy (RHT), to simplify the treatment in one-step two-phase treatment. Another non-Clarithromycin non-Bismuth quadruple therapy that is less complex and safer than bismuth quadruple therapy, which is called Levofloxacin quadruple therapy that contains levofloxacin, omeprazole, nitazoxanide, and doxycycline (LOND), showed promising results on the level of the cure rate and low drug resistance profile. Methods: Technical Design: A) The site of study: The study was conducted in Internal medicine department clinic in Zagazig University Hospitals. B) Sample size: Assuming that the eradication rate in patients receiving Hybrid therapy is 91% versus 78.3% in Reverse Hybrid therapy. So, the sample size is 309, using OPEN EPI at power 80% and C.I 95%. Tools of data collection: Medical history to all participants. Complete clinical examination. The fecal antigen test (FAT) which identifies H. pylori antigen in the stool by enzyme immunoassay was positive in all participants. Operational design: A) This is a randomized (interventional) study conducted at Zagazig University Hospital, internal medicine department clinic after informed consent. All the participants were positive for H. pylori fecal antigen test. B) Steps of performance: (330) participants were chosen from the Internal Medicine Department clinic, grouped into 3 groups: Group 1: (110) participants received reverse hybrid regimen in the form of clarithromycin 500mg bid, omeprazole 20 mg bid, amoxicillin 1gm bid, and metronidazole 500 mg tid for 1 week, followed by omeprazole 20 mg bid, and amoxicillin 1gm bid in the 2nd week. Group2: (110) participants received hybrid regimen in the form of omeprazole 20 mg bid, and amoxicillin 1gm bid in the 1st week, then clarithromycin 500mg bid, omeprazole 20 mg bid, amoxicillin 1gm bid, and metronidazole 500 mg tid in the 2nd week. Group3: (110) participants received Levofloxacin quadruple regimen (LOAD) in the form of nitazoxanide 500 mg bid, levofloxacin 250 mg QD, omeprazole 40 mg QD, and doxycycline 100 mg QD for 10 days C) Retesting by The fecal antigen test (FAT) after stopping the regimen by at least one month and withholding proton pump inhibitors for four weeks.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
This is a randomized controlled (interventional) study conducted at Zagazig University Hospital, internal medicine department clinic
Masking
None (Open Label)
Allocation
Randomized
Enrollment
330 (Actual)

8. Arms, Groups, and Interventions

Arm Title
(1) Hybrid regimen
Arm Type
Active Comparator
Arm Description
omeprazole 20mg bid, and amoxicillin 1gm bid in the 1st week, then clarithromycin 500mg bid, omeprazole 20mg bid, amoxicillin 1gm bid, and metronidazole 500mg tid in the 2nd week.
Arm Title
(2) Reverse hybrid regimen
Arm Type
Active Comparator
Arm Description
clarithromycin 500mg bid, omeprazole 20mg bid, amoxicillin 1gm bid, and metronidazole 500mg tid for 1 week, followed by omeprazole 20mg bid, and amoxicillin 1gm bid in the 2nd week.
Arm Title
(3) Levofloxacin quadruple regimen
Arm Type
Active Comparator
Arm Description
levofloxacin 250mg QD, omeprazole 40mg QD, nitazoxanide 500mg bid, and doxycycline 100mg QD for 10 days. (LOAD)
Intervention Type
Drug
Intervention Name(s)
Hybrid regimen
Intervention Description
two-step (dual-quadruple) treatment
Intervention Type
Drug
Intervention Name(s)
Reverse hybrid regimen
Intervention Description
one-step two-phase (quadruple-dual) treatment
Intervention Type
Drug
Intervention Name(s)
Levofloxacin quadruple regimen
Intervention Description
non-Clarithromycin non-Bismuth quadruple therapy
Primary Outcome Measure Information:
Title
Percentage of Helicobacter Pylori Infection Cure
Description
Measuring the curative rate of each regimen by a fecal antigen test
Time Frame
40-44 days
Title
Incidence of Treatment-Emergent Adverse Events
Description
Questionnaire to measure the number of Participants with Treatment-Emergent Adverse Events
Time Frame
10-14 days
Secondary Outcome Measure Information:
Title
Rate of Helicobacter Pylori Treatment Completion
Description
Questionnaire to evaluate the compliance with each treatment regimen
Time Frame
10-14 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Positive Helicobacter pylori antigen in the stool Treatment-naive Exclusion Criteria: Previous treatment for Helicobacter pylori Drug hypersensitivity
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ayman MM Sadek, MD
Organizational Affiliation
Zagazig University
Official's Role
Study Director
Facility Information:
Facility Name
Faculty of Human Medicine, Zagazig University
City
Zagazig
State/Province
Sharkia
ZIP/Postal Code
44519
Country
Egypt

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Time Frame
After study publication
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Comparison Between Quadruple Regimens for Helicobacter Pylori Infection in Egypt

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