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Comparison of Efficacy of Triple Regimen Based on Clarithromycin VS Metronidazole in Children (CETR)

Primary Purpose

H Pylori Gastritis

Status
Unknown status
Phase
Not Applicable
Locations
Pakistan
Study Type
Interventional
Intervention
Clarithromycin+ Amoxicillin + Omeprazole
Metronidazole +Amoxicillin + Omeprazole
Sponsored by
Shaheed Zulfiqar Ali Bhutto Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for H Pylori Gastritis focused on measuring H-pylori gastritis, eradication therapy, triple regimen

Eligibility Criteria

1 Year - 12 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 1. All children age 1-12 years having H-pylori gastritis

Exclusion Criteria:

  • drug induced gastritis critically ill child

Sites / Locations

  • Pakistan Institute of Medical Sciences,SZABMURecruiting
  • Pakistan Institute of Medical Sciences, IslamabadRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Group A

Group B

Arm Description

Group A will be given Amoxicillin AMO + Clarithromycin CLA + Proton pump inhibitor PPI based triple regimen

Group B will be given Amoxicillin AMO+ Metronidazole MET+ Proton pump inhibitor PPI based triple regimen

Outcomes

Primary Outcome Measures

Efficacy of Clarithromycin vs Metronidazole based triple regimen in treatment of H-pylori in induced Acid peptic disease in children in terms of reduction in duration of symptoms and negative Stool H-Pylori-Ag
All children age 1-12 years diagnosed with acid peptic disease with positive H-pylori Ag in stool will be randomized in to Group A & Group B and will be given either CLA or MET based triple eradication regimen. After 4 weeks of complication of triple regimen patients form both groups will be re-tested for H-pylori Ag in stool. The efficacy of both regimen will be compare in terms of duration of resolution of symptoms of Acid peptic disease and number of patients having negative stool H pylori Ag post treatment.

Secondary Outcome Measures

Full Information

First Posted
January 16, 2021
Last Updated
January 22, 2021
Sponsor
Shaheed Zulfiqar Ali Bhutto Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT04721704
Brief Title
Comparison of Efficacy of Triple Regimen Based on Clarithromycin VS Metronidazole in Children
Acronym
CETR
Official Title
Comparison of Efficacy and Safety of Triple Regimen Based on Clarithromycin VS Metronidazole in Pediatric Population in Pakistan
Study Type
Interventional

2. Study Status

Record Verification Date
January 2021
Overall Recruitment Status
Unknown status
Study Start Date
September 14, 2020 (Actual)
Primary Completion Date
September 14, 2022 (Anticipated)
Study Completion Date
September 14, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shaheed Zulfiqar Ali Bhutto Medical University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
All children from 1day to 18years of age, diagnosed with peptic ulcer disease due to H pylori at Pakistan Institute of Medical Sciences, Islamabad, from July 2020 to December 2021 will be included in the study. After informed written consent from parents/ guardians patients' bio data along with history and examination will be recorded on a proforma. They will be allocated into two groups, group A and group B randomly based on treatment regimen offered. Group A: Amoxicillin AMO + Clarithromycin CLA + Proton pump inhibitor PPI) Group B: Amoxicillin AMO+ Metronidazole MET+ Proton pump inhibitor PPI The history will include presenting symptoms along duration, remission of symptoms after therapy and clinical outcome will also be recorded.
Detailed Description
Helicobacter pylori is a gram-negative bacillus responsible for one of the most common infections found in humans worldwide1. In general, the prevalence is high in developing countries and the infection is acquired at a young age. Most children infected with H pylori are asymptomatic. Antral gastritis is the most common manifestation in children. Duodenal and gastric ulcers may be associated with H pylori gastritis in 1.8 % children2. Antibiotic resistance is the major cause of failure in the treatment of H pylori infection3. Most of the studies worldwide confirmed an increase in macrolide resistance, while metronidazole resistance either decreased or remained stable. In a prospective multicenter European study, primarily comprised of adults, found a 31.8% resistance rate to clarithromycin and 25.7% to metronidazole in the study4. If the strain is resistant to one of the antibiotics used, treatment success will be compromised5. As a result therapies that are recommended should be based on antibiotic susceptibility testing. If this testing is not available, then clarithromycin-based triple therapy should not be used as part of first-line therapy due to high rates of clarithromycin resistance rates6 The European Society for Paeditric Gastroenterology Hepatology and Nutrition/North American Society for Pediatric Gastroenterology, Hepatology and Nutrition made the recommendations in 2017 for the Management of Helicobacter pylori in Children that antimicrobial sensitivity should be obtained for the infecting H pylori to tailor eradication therapy accordingly and the effectiveness of first-line therapy should be evaluated in national/regional centers7. If the strain is susceptible to clarithromycin (CLA) and to metronidazole (MET), triple therapy (PPI, amoxicillin [AMO], CLA) for 14 days and doses of proton pump inhibitor and antibiotics should be calculated based on the bodyweight8. We aim to study efficacy and safety of clarithromycin vs metronidazole based triple regimen for the eradication of H pylori in children with peptic ulcer disease.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
H Pylori Gastritis
Keywords
H-pylori gastritis, eradication therapy, triple regimen

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
36 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Group A
Arm Type
Experimental
Arm Description
Group A will be given Amoxicillin AMO + Clarithromycin CLA + Proton pump inhibitor PPI based triple regimen
Arm Title
Group B
Arm Type
Experimental
Arm Description
Group B will be given Amoxicillin AMO+ Metronidazole MET+ Proton pump inhibitor PPI based triple regimen
Intervention Type
Drug
Intervention Name(s)
Clarithromycin+ Amoxicillin + Omeprazole
Other Intervention Name(s)
Klaricid + Amoxil + Risek
Intervention Description
In Group A: Amoxicillin AMO + Clarithromycin CLA + Proton pump inhibitor PPI will be given to children
Intervention Type
Drug
Intervention Name(s)
Metronidazole +Amoxicillin + Omeprazole
Other Intervention Name(s)
Flagyl + Amoxil + Risek
Intervention Description
Group B: Amoxicillin AMO+ Metronidazole MET+ Proton pump inhibitor PPI
Primary Outcome Measure Information:
Title
Efficacy of Clarithromycin vs Metronidazole based triple regimen in treatment of H-pylori in induced Acid peptic disease in children in terms of reduction in duration of symptoms and negative Stool H-Pylori-Ag
Description
All children age 1-12 years diagnosed with acid peptic disease with positive H-pylori Ag in stool will be randomized in to Group A & Group B and will be given either CLA or MET based triple eradication regimen. After 4 weeks of complication of triple regimen patients form both groups will be re-tested for H-pylori Ag in stool. The efficacy of both regimen will be compare in terms of duration of resolution of symptoms of Acid peptic disease and number of patients having negative stool H pylori Ag post treatment.
Time Frame
2 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 1. All children age 1-12 years having H-pylori gastritis Exclusion Criteria: drug induced gastritis critically ill child
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Nadia Waheed
Phone
923334461116
Email
drnadiasalman@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Nighat Haider
Phone
923212125768
Email
nighathaider@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nadia Waheed
Organizational Affiliation
PIMS, SZABMU,ISLAMABAD
Official's Role
Principal Investigator
Facility Information:
Facility Name
Pakistan Institute of Medical Sciences,SZABMU
City
Islamabad
State/Province
Capital Territory
ZIP/Postal Code
44000
Country
Pakistan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nadia W,aheed, FCPS
Phone
923334461116
Email
drnadiasalman@gmail.com
First Name & Middle Initial & Last Name & Degree
Nighat Haider, FCPS
Phone
923212125768
Email
nighathaider@hotmail.com
First Name & Middle Initial & Last Name & Degree
Jai Krishin, FCPS
Facility Name
Pakistan Institute of Medical Sciences, Islamabad
City
Islamabad
State/Province
Islamabad Capital Territory
ZIP/Postal Code
44000
Country
Pakistan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nadia W,aheed, FCPS
Phone
923334461116
Email
drnadiasalman@gmail.com
First Name & Middle Initial & Last Name & Degree
Nighat Haider, FCPS
Phone
923212125768
Email
nighathaider@hotmail.com
First Name & Middle Initial & Last Name & Degree
Jai Krishin, FCPS

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
SPSS DATA SHEETS WILL BE SHARED
IPD Sharing Time Frame
6 months after publication for further 6 months
IPD Sharing Access Criteria
through email on demand

Learn more about this trial

Comparison of Efficacy of Triple Regimen Based on Clarithromycin VS Metronidazole in Children

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