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

Sponsor
Shaheed Zulfiqar Ali Bhutto Medical University (Other)
Overall Status
Recruiting
CT.gov ID
NCT04721704
Collaborator
(none)
36
2
2
24
18
0.8

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Drug: Clarithromycin+ Amoxicillin + Omeprazole
  • Drug: Metronidazole +Amoxicillin + Omeprazole
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
36 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Comparison of Efficacy and Safety of Triple Regimen Based on Clarithromycin VS Metronidazole in Pediatric Population in Pakistan
Actual Study Start Date :
Sep 14, 2020
Anticipated Primary Completion Date :
Sep 14, 2022
Anticipated Study Completion Date :
Sep 14, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Group A

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

Drug: Clarithromycin+ Amoxicillin + Omeprazole
In Group A: Amoxicillin AMO + Clarithromycin CLA + Proton pump inhibitor PPI will be given to children
Other Names:
  • Klaricid + Amoxil + Risek
  • Experimental: Group B

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

    Drug: Metronidazole +Amoxicillin + Omeprazole
    Group B: Amoxicillin AMO+ Metronidazole MET+ Proton pump inhibitor PPI
    Other Names:
  • Flagyl + Amoxil + Risek
  • Outcome Measures

    Primary Outcome Measures

    1. 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 [2 weeks]

      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.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    1 Year to 12 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
      1. All children age 1-12 years having H-pylori gastritis
    Exclusion Criteria:
    • drug induced gastritis critically ill child

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Pakistan Institute of Medical Sciences,SZABMU Islamabad Capital Territory Pakistan 44000
    2 Pakistan Institute of Medical Sciences, Islamabad Islamabad Islamabad Capital Territory Pakistan 44000

    Sponsors and Collaborators

    • Shaheed Zulfiqar Ali Bhutto Medical University

    Investigators

    • Principal Investigator: Nadia Waheed, PIMS, SZABMU,ISLAMABAD

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Dr.Nadia waheed, Assistant professor, Shaheed Zulfiqar Ali Bhutto Medical University
    ClinicalTrials.gov Identifier:
    NCT04721704
    Other Study ID Numbers:
    • F-.1-1/2015/ERB/SZABMU/646
    First Posted:
    Jan 25, 2021
    Last Update Posted:
    Jan 26, 2021
    Last Verified:
    Jan 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    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
    Keywords provided by Dr.Nadia waheed, Assistant professor, Shaheed Zulfiqar Ali Bhutto Medical University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 26, 2021