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A prospective multicenter, randomized, controlled clinical study on the efficacy of quadruple regimens containing PPI, cefuroxime, minocycline and bismuth for eradication of Helicobacter pylori

A prospective multicenter, randomized, controlled clinical study on the efficacy of quadruple regimens containing PPI, cefuroxime, minocycline and bismuth for eradication of Helicobacter pylori

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000040812
Enrollment
Unknown
Registered
2020-12-10
Start date
2020-12-15
Completion date
Unknown
Last updated
2021-04-12

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

Conditions

Helicobacter pylori infecion

Interventions

A:Minocycline (100mg twice a day) + Cefuroxime (500mg,twice a day) + Bismuth (220mg, twice a day) + Esomeprazole (20mg, twice a day) for two weeks
B:Minocycline (100mg twice a day) + Axoxicillin (500mg, twice a day) + Bismuth (220mg, twice a day) + Esomeprazole (20mg, twice a day) for two weeks
C:Clarithromycin (500mg twice a day) + Axoxicillin (500mg, twice a day) + Bismuth (220mg, twice a day) + Esomeprazole (20mg, twice a day) for two weeks

Sponsors

Fujian Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Adult patients, aged between 18-70 years. 2. Patients who did not take antibiotics, bismuth and traditional Chinese medicine 4 weeks before treatment, and patients who took PPI, H2 receptor antagonists and other drugs that affect HP activity 2 weeks before treatment; 3. Patients who were diagnosed as HP positive by C13 or C14 urea breath test, rapid urease test and histopathology, and who had not received HP eradication treatment before; 4. Informed and agreed to participate in the study, patients with complete medical records and follow-up records.

Exclusion criteria

Exclusion criteria: 1. With severe heart, lung, and kidney dysfunction and low immunity; 2. Patients with drug allergy contraindications; 3. Persons with mental illness or communication difficulties; 4. Pregnancy, lactation; 5. Patients with organic diseases such as gastrointestinal tumor and gastrointestinal hemorrhage.

Design outcomes

Primary

MeasureTime frame
eradication rate;

Secondary

MeasureTime frame
antibiotic resistance of Helicobacter pylori;adverse reaction;

Countries

China

Contacts

Public ContactZhihui Lin

Fujian Provincial Hospital

303622465@qq.com+86 15750819302

Outcome results

None listed

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