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The Efficacy and Safety of Anaprazole Quadruple Therapy Versus Rabeprazole Quadruple Therapy for Helicobacter pylori Eradication: A Prospective, Multicenter, Open-label, Randomized Controlled Clinical Study

The Efficacy and Safety of Anaprazole Quadruple Therapy Versus Rabeprazole Quadruple Therapy for Helicobacter pylori Eradication: A Prospective, Multicenter, Open-label, Randomized Controlled Clinical Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600117235
Enrollment
Unknown
Registered
2026-01-21
Start date
2026-01-27
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Helicobacter pylori gastritis

Interventions

Group A:Anaprazole + Amoxicillin + Furazolidone + Colloidal Bismuth Pectin
Group B:Rabeprazole + Amoxicillin + Furazolidone + Colloidal Bismuth Pectin

Sponsors

NanJing First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Aged 18-65 years ; 2.Patients with a positive 13C or 14C breath test who have not received prior H. pylori eradication therapy; 3.Voluntary enrolment and informed consent.

Exclusion criteria

Exclusion criteria: 1.Those who are allergic to the drugs used in the eradication programme; 2.Patients with recent bleeding from gastroduodenal ulcers or signs of bleeding within the past 4 weeks; 3.Patients with a history of Helicobacter pylori eradication therapy; 4.Use of antibiotics or bismuth within 4 weeks prior to the initiation of study treatment, or use of histamine H2-receptor antagonists (H2RAs) or proton pump inhibitors (PPIs) within 2 weeks prior to the initiation of study treatment. (Note: This translation maintains the medical terminology and accurately reflects the timeframes for medication restrictions before starting the study.); 5.Use of corticosteroids, nonsteroidal anti-inflammatory drugs (NSAIDs), or anticoagulants. 6.Patients with a history of esophageal or gastric surgery; 7.Pregnant or lactating women; 8.Patients with concurrent severe physical or mental illnesses, or hepatic/renal dysfunction; 9.Patients with gastric mucosa-associated lymphoid tissue (MALT) lymphoma or malignant tumors. 10.Patients with glucose-6-phosphate dehydrogenase (G6PD) deficiency, peptic ulcer disease, or bronchial asthma. 11.Has the following comorbid medications: atazanavir or rilpivirine, tricyclic antidepressants, levodopa, acetaminophen, guaifenesin/dextromethorphan, monoamine oxidase inhibitors, tramadol, and others.

Design outcomes

Primary

MeasureTime frame
Eradication rate;

Secondary

MeasureTime frame
Incidence of adverse reactions;Patient compliance;

Countries

China

Contacts

Public ContactZhang Zhenyu

NanJing First Hospital

zzy6565@sina.com+86 25 52271000

Outcome results

None listed

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