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Clinical study of Weierkang pills combined with triple therapy for Helicobacter pylori infection

Clinical study of Weierkang pills combined with triple therapy for Helicobacter pylori infection

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2000003109
Enrollment
Unknown
Registered
2020-03-14
Start date
2020-04-01
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

Heilicobacter pylori infection

Interventions

Sponsors

Department of Gastroenterology, Run Run Shaw Hospital of Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Voluntarily sign the informed consent; 2. The age is more than 18 years old, men and women are not limited; 3. Patients who were Hp positive without anti-bacterial treatment;

Exclusion criteria

Exclusion criteria: 1. Patients who have used antibiotics or bismuth agent within 4 weeks; Patients who had used antacids (H2 antagonists or proton pump inhibitors), prokinetic drugs (mosapride or doperidone, etc.) and gastric mucosa protectants (tipredone, sucralose, rabapet, etc.) in the previous 2 weeks; 2. Patients with serious lesions in important organs of the body (heart, liver, kidney, lung, etc.); 3. Patients diagnosed with gastric cancer by gastroscopy or other examinations; 4. Pregnant and nursing women; 5. Unable to follow visitors or allergic to this study.

Design outcomes

Primary

MeasureTime frame
Hp eradication rate;Incidence of adverse reactions;

Secondary

MeasureTime frame
Symptom remission rate;

Countries

China

Contacts

Public ContactHu Weiling

Department of Gastroenterology, Run Run Shaw Hospital of Zhejiang University School of Medicine

huweiling@zju.edu.cn+86 13516800685

Outcome results

None listed

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