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Lactobacillus reuteri Supplementation for Helicobacter pylori Eradication among Patients with Dyspepsia

Lactobacillus reuteri Supplementation versus Standard Triple Therapy for Helicobacter pylori Eradication among Patients with Dyspepsia

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20141201020178N10
Enrollment
80
Registered
2020-09-11
Start date
2020-05-16
Completion date
Unknown
Last updated
2020-10-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Condition 1: Functional dyspepsia. Condition 2: Helicobacter pylori. Functional dyspepsia Helicobacter pylori [H. pylori] as the cause of diseases classified elsewhere

Interventions

Intervention 1: Intervention group: Esomeperazole Cap 40 mg BD + Amoxicillin Cap 500 mg 2*BD + Clarithromycin Tab 500 mg BD + Pyloshot Tab for 10 days. Intervention 2: Control group: Esomeperazole Cap

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Patients aged between 18 to 70 years old with dyspepsia presentation H. Pylori documentation by antral biopsy (Rapid Urease Test or Giemsa staining) or Urea Breath Test

Exclusion criteria

Exclusion criteria: Pregnancy or breast- feeding Women taking oral contraceptive pill (OCP) Significant underlying diseases such as cardiac, pulmonary, renal, liver, endocrine, central nervous system (CNS) diseases and cancers Previous history of gastric surgery Patients taking triple therapy for H. Pylori eradication History of taking proton pump inhibitor (PPI), histamine H2- receptor blocker (H2B) or antibiotic during previous two weeks Concomitant use of anticoagulant or corticosteroid Previous history of taking monoamine oxidase (MAO) inhibitors or tricyclic antidepressants (TCA)

Design outcomes

Primary

MeasureTime frame
Helicobacter Pylori eradication rate. Timepoint: Six weeks after the end of therapy. Method of measurement: Stool Antigen Test.

Secondary

MeasureTime frame
Rate of supplementation's side effects. Timepoint: After end of the therapy. Method of measurement: Patients' follow-up checklist.;Patient's compliance rate. Timepoint: After end of the therapy. Method of measurement: Patients' follow-up checklist.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMarjan Mokhtare

Iran University of Medical Sciences

mokhtare.m@iums.ac.ir+98 21 6735 2477

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 6, 2026