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Clinical study on the clinical effect of Saccharomyces boulardii-assisted standard bismuth quadruple therapy in patients with Helicobacter pylori infection

Clinical study on the clinical effect of Saccharomyces boulardii-assisted standard bismuth quadruple therapy in patients with Helicobacter pylori infection

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123337
Enrollment
Unknown
Registered
2026-04-24
Start date
2026-04-30
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

Helicobacter pylori infection

Interventions

Control group:The control group will receive the standard bismuth quadruple therapy
experimental group:the experimental group will add the Bovis yeast powder to the standard bismuth quadruple therapy

Sponsors

The First Affiliated Hospital of Xinjiang Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years, any gender. 2. Patients diagnosed with confirmed H. pylori infection, confirmed by gastric biopsy rapid urease test (RUT) or ^13C/^14C urea breath test (UBT) through endoscopy. 3. Meet the treatment standards recommended by the "Sixth National Consensus Report on Helicobacter pylori Infection Management" and meet the indications for standard bismuth quadruple therapy. 4. Subjects voluntarily sign the informed consent form, can follow up on time, and adhere to the treatment plan. 5. Have not previously received formal H. pylori treatment.

Exclusion criteria

Exclusion criteria: 1. History of gastrectomy, gastric cancer, or other malignant tumors. 2. Severe cardiac, hepatic, or renal dysfunction, or having immune system diseases (such as HIV infection or autoimmune diseases). 3. Recent use of antibiotics, bismuth agents, probiotics, or PPIs that may affect Hp test results. 4. Allergy-prone individuals or those with a history of allergy to study drugs (amoxicillin, clarithromycin, bismuth agents, Saccharomyces boulardii). 5. Past or current pyloric obstruction, gastrointestinal perforation, or hemorrhagic diseases, or concomitant severe gastrointestinal diseases (such as Crohn's disease or ulcerative colitis). 6. Pregnant or breastfeeding women, or those planning pregnancy. 7. Poor compliance, unable to complete study follow-up or medication regimen on time.

Design outcomes

Secondary

MeasureTime frame
HP eradication rate;Incidence of adverse reactions and symptom relief;Inflammatory cytokine levels;Pepsinogen levels;

Countries

China

Contacts

Public ContactZhang Zhiqiang

The First Affiliated Hospital of Xinjiang Medical University

drzhiqiang@163.com+86 137 0991 9966

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026