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Study for the efficacy of probiotics combined to Modified Dual Therapy for refractory Helicobacter pylori infection

Study for the efficacy of probiotics combined to Modified Dual Therapy for refractory Helicobacter pylori infection

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034004
Enrollment
Unknown
Registered
2020-06-21
Start date
2020-07-01
Completion date
Unknown
Last updated
2020-06-22

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

Conditions

refractory helicobacter pylori infection

Interventions

experimental group:probiotics combined to Modified Dual Therapy
control group:Phased integrated therapy

Sponsors

People's Hospital of Shapingba district of Chongqing
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) from July 2020 to July 2022, patients aged 18-65 years old, male or female, will visit the outpatient and inpatient departments of the department of gastroenterology, chongqing shapingba district people's hospital; (2) meet the standard of refractory helicobacter pylori infection: the number of treatment failures of bismuth quadruplex therapy within 3 years with normal and full course of treatment (>=10 days) >=3 times; (3) chronic gastritis confirmed by gastroscopy, with or without healed gastric ulcer or duodenal bulbus ulcer;Rapid urease test (RUT) and 14c-urea breath test (14c-ubt) proved positive for HP infection; To be included, patients who meet each of the above criteria must sign an informed consent.

Exclusion criteria

Exclusion criteria: In the first four weeks of treatment, I have used PPI,H2 Receptor antagonists (H2RAs), antibiotics, traditional Chinese medicine containing antibacterial effects, bismuth, probiotics and other drugs.Pregnant or lactating women, patients with family planning during the study period;Alcohol abuse;At the same time take non - steroidal anti - inflammatory drugs, adrenocorticosteroids, anticoagulants;Allergic to the drugs used in this study;Severe concomitant diseases, such as heart disease, lung disease, liver disease, kidney disease, metabolic disease, mental disease, malignant tumor, etc. Previous gastric and esophageal surgery, or gastric mucosa with high-grade intraepithelial neoplasia;Difficulty in completing follow-up or the presence of other factors affecting compliance.The above standard accords with one item to want to exclude namely.

Design outcomes

Primary

MeasureTime frame
Clinical efficacy of drugs;

Secondary

MeasureTime frame
adverse drug reaction;patient compliance;factors affecting the rate of therapeutic eradication;

Countries

China

Contacts

Public ContactYang Fan

People's Hospital of Shapingba district of Chongqing

787838896@qq.com+86 18523857287

Outcome results

None listed

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