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Study on the efficacy and mechanism of the combination therapy of probiotics and dead cells in the treatment of Helicobacter pylori

Study on the efficacy and mechanism of the combination therapy of probiotics and dead cells in the treatment of Helicobacter pylori

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086736
Enrollment
Unknown
Registered
2024-07-09
Start date
2024-07-20
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

helicobacter pylori infection

Interventions

Combination of probiotics and triple therapy group:Composite probiotics: 1 probiotic per day, taken orally directly, or delivered with warm water (50ml, below 40 degrees), taken after meals
Triple use: Amoxicillin: 2g/dose, bid, take half an hour after breakfast and dinner
Clarithromycin: 0.5g/dose, bid, taken half an hour after breakfast and dinner
Rabeprazole: 20mg/dose, bid, taken half an hour before breakfast, dinner, and meals.
Bismuth quadruple combined with placebo treatment group:Placebo: 1 tablet per day, taken orally or with warm water (50ml, below 40 degrees), taken after meals
Quadruple usage: Amoxicillin: 2g/dose, bid, taken half an hour after breakfast and dinner
Rabeprazole: 20mg/dose, bid, taken half an hour before breakfast, dinner, and meals
Potassium bismuth citrate: 0.6g/dose, bid, taken half an hour before breakfast and dinner.
Dead cell combination triple therapy group:Dead cell count: 1 piece/day, taken orally or in warm water (50ml, below 40 degrees), taken after meals

Sponsors

Inner Mongolia Autonomous Region People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Voluntarily sign an informed consent form; 2. No gender limit, age 18-70 years old; 3. Positive 14C urea breath test (14C-UBT), with no prior treatment for Helicobacter pylori; 4. Have not used antibiotics, bismuth or probiotic related preparations in the month prior to enrollment;

Exclusion criteria

Exclusion criteria: 1. Subjects who have previously treated Helicobacter pylori; 2. Pregnant, pregnant or lactating women; 3. Individuals who have taken antibiotics, proton pump inhibitors, H2 receptor antagonists, bismuth preparations, and certain antibacterial drugs 4 weeks prior to enrollment; 4. Patients with a history of major gastrointestinal surgery or complications such as bleeding, perforation, obstruction, and cancer; 5. Patients with a history of drug allergies or contraindications; 6. Other serious illnesses;

Design outcomes

Primary

MeasureTime frame
14c-urea breath test;

Secondary

MeasureTime frame
Inflammatory factor detection;Functional indicators of intestinal mucosa;Intestinal flora;Oral flora;Serum metabolome;Serological indicators;gastric microbiota;

Countries

China

Contacts

Public ContactYan Li

Inner Mongolia Autonomous Region People's Hospital

978303387@qq.com+86 180 0481 3900

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026