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Enrolling by invitation Phase 4

The Efficacy of 10-day and 14-day Bismuth-based Quadruple Therapy in First-line H. Pylori Eradication

NCT04527055 · tracked via the Priya Life Science Taiwan tracker
Phase
Phase 4
Started
2020-05-06
Last updated
2024-06-24

Condition(s) studied

Helicobacter Pylori InfectionDysbiosisProbiotics

Investigational drug(s) / intervention(s)

Bismuth Subcitrate 120 MG Oral Tablet →Lactobacillus acidophilus and Bifidobacterium lactis Bb12Esomeprazole 40mg →Metronidazole 250 MG →Tetracycline Pill →

Bismuth Subcitrate 120 MG Oral Tablet: Bismuth Subcitrate (120 MG Oral Tablet) 1 tab per oral four times per day for 14 days in the14-day bismuth-based quadruple therapy and for 10 days in the10-day bismuth-based quadruple therapy

Lactobacillus acidophilus and Bifidobacterium lactis Bb12: The probiotic powder per oral twice daily for 24 weeks. The probiotic powder is named as "President AB powder", which contains an approximately equal mixture of Lactobacillus acidophilus and Bifidobacterium lactis Bb12 at a concentration of \>= 10E9 CFU/mL (President Corp., Tainan, Taiwan).

Esomeprazole 40mg: Esomeprazole (40 mg) 1 tab per oral twice per day for 14 days in the14-day bismuth-based quadruple therapy and for 10 days in the10-day bismuth-based quadruple therapy

Metronidazole 250 MG: Metronidazole (250 MG) 2 tab per oral thrice per day for 14 days in the14-day bismuth-based quadruple therapy and for 10 days in the10-day bismuth-based quadruple therapy

Tetracycline Pill: Tetracycline (250 MG) 2 tab per oral four times per day for 14 days in the14-day bismuth-based quadruple therapy and for 10 days in the10-day bismuth-based quadruple therapy

Study summary

Helicobacter pylori (H. pylori) infection is the major cause of gastritis, peptic ulcer disease, and gastric cancer in adults. Bismuth-based quadruple therapy is recommended by a recent review to be the first-line treatment for H. pylori eradication, replacing clarithromycin-based triple therapy. It is because the eradication rates of triple therapy in adults have declined due to increasing clarithromycin resistance. The best regimen for H. pylori eradication should be the one which succeeds on the first attempt. However, the effectiveness and the optimal duration of bismuth-based quadruple therapy for first-line H. pylori eradication in adults are unknown. Moreover, the impacts on gut microbiota after H. pylori eradication should be concerned; for example, bismuth-based quadruple therapy decreases F. prausnitzii richness. The transient perturbation of the gut microbiota after H. pylori eradication were restored at 8 weeks and one year in subjects receiving clarithromycin-based triple therapy but not fully recovered in those receiving bismuth-based quadruple therapy. Therefore, the important issues are that the short-term and long-term gut dysbiosis and the recovery of gut F. prausnitzii depletion in H. pylori-infected adult patients after bismuth-based quadruple therapy. It is also uncertain the role of irreversible gut dysbiosis even though H. pylori is eradicated in gastric persist inflammation and progress to cancer, and whether probiotics could be helpful in recovering gut dysbiosis.

The therapeutic strategy to eradicate H. pylori infection is based on antibiotics; however, this strategy not only increases drug resistant rates of the pathogen but also shapes the gut microbiota.

The investigators hypothesize that bismuth-based quadruple therapy could be an optimal regimen for first-line H. pylori eradication in the era of increasing clarithromycin resistance; moreover, gut dysbiosis could be reversed after bismuth-based quadruple therapy. Furthermore, the efficacy of the10-day course is not inferior to that of the 14-day course in H. pylori eradication. The investigators also hypothesize that probiotics could restore gastric or gut dysbiosis, especially gut F. prausnitzii depletion.

Eligibility

Sex
ALL
Min age
18 Years
Max age
100 Years
Healthy volunteers
No
Inclusion Criteria: * Patients who are \> 18 years * Receive gastroscopy because of dyspepsia, acid regurgitation, melena, hematemesis, or others Exclusion Criteria: * Bleeding diathesis, * Major organic diseases * Malignancy * Diseases treated with chemotherapy within one month * Diseases treated with steroids within one month * Diseases treated with antibiotics within one month, * Users of aspirin within four weeks before enrollment * Users of nonsteroidal anti-inflammatory drugs within four weeks before enrollment * Users of cyclooxygenase-2 selective inhibitors within four weeks before enrollment * History of H. pylori eradication * Ingest probiotics or probiotics-containing yogurt with a frequency of \>= twice per week one month prior to enrollment

Primary outcome measure(s)

  • The successful eradication rate — About 4 to 6 weeks after receiving the H. pylori eradication regimen
    The patients stop taking the proton pump inhibitor and antibiotics for 4 to 6 weeks, and then they receive 13C-UBT or an H. pylori stool antigen test to confirm successful eradication or not.

Trial sites (1)

FacilityCityRegionStatus
Helicobacter pylori study group, National Cheng Kung University Hospital Tainan Taiwan
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04527055 on ClinicalTrials.gov ↗ ← All trials in Taiwan