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Recurrence Rate Comparison Between Esomeprazole and Lansoprazole in Eradicating Helicobacter Pylori Infection Among Children

Primary Purpose

Helicobacter Pylori Infection

Status
Completed
Phase
Phase 2
Locations
Indonesia
Study Type
Interventional
Intervention
Esomeprazole
Lansoprazole
Amoxicillin
Clarithromycin
Sponsored by
Finni Kollins
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, Triple therapy, Children, Esomeprazole, Lansoprazole

Eligibility Criteria

2 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Subject has positive clinical symptoms (gastrointestinal pain, nausea, vomiting, hematemesis, or melena) Subject had been diagnosed with H.pylori infection prior to endoscopy and rapid urease testing Exclusion Criteria: subject has a history of using antibiotics or non-steroidal anti-inflammatory medicines (NSAIDs) within 14 days prior to surgery subject has a concomitant systemic disease (e.g., renal failure, liver cirrhosis, cancer, etc.) that could theoretically affect the subject's response to treatment Incomplete triple pharmacologic treatment due to the subject's lack of medication adherence

Sites / Locations

  • Universitas Sumatera Utara General Hospital
  • Haji Adam Malik General Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Esomeprazole in combination with Amoxicillin and Clarithromycin

Lansoprazole in combination with Amoxicillin and Clarithromycin

Arm Description

Esomeprazole : once a day per oral; 0.4 mg/kg Amoxicillin: thrice a day per oral; 25 mg/kg Clarithromycin: twice a day per-oral; 7.5 mg/kg

Lansoprazole: once a day per oral; 15 mg if body weight < 30 kg and 30 mg if body weight > 30 kg Amoxicillin: thrice a day per oral; 25 mg/kg Clarithromycin: twice a day per-oral; 7.5 mg/kg

Outcomes

Primary Outcome Measures

Helicobacter pylori Stool Antigen Test
The stool of the subjects will be assessed on day-15 after drug administration. A negative result indicates that patient is infection-free

Secondary Outcome Measures

Helicobacter pylori Stool Antigen Test
The stool of the subjects will be analyzed on day-90 after drug administration to assess whether a reinfection is present. A negative result indicates that patient is infection-free

Full Information

First Posted
May 6, 2023
Last Updated
May 16, 2023
Sponsor
Finni Kollins
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1. Study Identification

Unique Protocol Identification Number
NCT05861687
Brief Title
Recurrence Rate Comparison Between Esomeprazole and Lansoprazole in Eradicating Helicobacter Pylori Infection Among Children
Official Title
Comparative Recurrence Rate Investigation of Esomeprazole Versus Lansoprazole in Triple-Combination Therapy to Eradicate Helicobacter Pylori Infection Among Pediatrics: Multicentre, Randomized, and Controlled Trials
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Completed
Study Start Date
August 1, 2021 (Actual)
Primary Completion Date
December 7, 2021 (Actual)
Study Completion Date
May 20, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Finni Kollins

4. Oversight

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

5. Study Description

Brief Summary
This study aims to compare the recurrence rates of Esomeprazole and Lansoprazole in triple combination therapy to eradicate H.pylori infection in children. The participants were divided into two groups, those who received Esomeprazole and those who received Lansoprazole
Detailed Description
H. pylori eradication therapy is still contentious. A treatment that is uncomplicated, well-tolerated, and boasts an efficiency rate of more than 80% is recommended. PPIs are a type of acid-sensitive drug which is most beneficial in preventing the degradation of drugs in the stomach. In developing countries, Esomeprazole and Lansoprazole were mainly selected as a drug of choice. Major influential factors such as Esomeprazole's additional antioxidant ability, are comparable to vitamin C. This is due to its ability to scavenge Diphenyl Picrylhydrazyl (DPPH) free radicals at low concentrations. Lansoprazole also possess similar ability, albeit needs a slightly higher concentration to reach a similar effect. In terms of IC50 values, both drugs have a substantial advantage over vitamin C, earning them the title of 'potentially ideal' agents in the treatment algorithm. Furthermore, numerous studies mention that children better tolerate PPIs.

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, Triple therapy, Children, Esomeprazole, Lansoprazole

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
51 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Esomeprazole in combination with Amoxicillin and Clarithromycin
Arm Type
Experimental
Arm Description
Esomeprazole : once a day per oral; 0.4 mg/kg Amoxicillin: thrice a day per oral; 25 mg/kg Clarithromycin: twice a day per-oral; 7.5 mg/kg
Arm Title
Lansoprazole in combination with Amoxicillin and Clarithromycin
Arm Type
Active Comparator
Arm Description
Lansoprazole: once a day per oral; 15 mg if body weight < 30 kg and 30 mg if body weight > 30 kg Amoxicillin: thrice a day per oral; 25 mg/kg Clarithromycin: twice a day per-oral; 7.5 mg/kg
Intervention Type
Drug
Intervention Name(s)
Esomeprazole
Intervention Description
Administered once a day per-oral (PO) with the dose of 0.4 mg/kg
Intervention Type
Drug
Intervention Name(s)
Lansoprazole
Intervention Description
Administered once a day per-oral (PO) with the dose of 15 mg if individual's body mass was <30 kg, and 30 mg if it was >30 kg
Intervention Type
Drug
Intervention Name(s)
Amoxicillin
Intervention Description
Administered thrice a day per-oral (PO) with the dose of 25 mg/kg
Intervention Type
Drug
Intervention Name(s)
Clarithromycin
Intervention Description
Administered twice a day per-oral with the dose of 7.5 mg/kg
Primary Outcome Measure Information:
Title
Helicobacter pylori Stool Antigen Test
Description
The stool of the subjects will be assessed on day-15 after drug administration. A negative result indicates that patient is infection-free
Time Frame
15 days
Secondary Outcome Measure Information:
Title
Helicobacter pylori Stool Antigen Test
Description
The stool of the subjects will be analyzed on day-90 after drug administration to assess whether a reinfection is present. A negative result indicates that patient is infection-free
Time Frame
75 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subject has positive clinical symptoms (gastrointestinal pain, nausea, vomiting, hematemesis, or melena) Subject had been diagnosed with H.pylori infection prior to endoscopy and rapid urease testing Exclusion Criteria: subject has a history of using antibiotics or non-steroidal anti-inflammatory medicines (NSAIDs) within 14 days prior to surgery subject has a concomitant systemic disease (e.g., renal failure, liver cirrhosis, cancer, etc.) that could theoretically affect the subject's response to treatment Incomplete triple pharmacologic treatment due to the subject's lack of medication adherence
Facility Information:
Facility Name
Universitas Sumatera Utara General Hospital
City
Medan
State/Province
North Sumatera
ZIP/Postal Code
20124
Country
Indonesia
Facility Name
Haji Adam Malik General Hospital
City
Medan
State/Province
North Sumatera
ZIP/Postal Code
20136
Country
Indonesia

12. IPD Sharing Statement

Plan to Share IPD
No
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Recurrence Rate Comparison Between Esomeprazole and Lansoprazole in Eradicating Helicobacter Pylori Infection Among Children

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