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A comparative study of optional dule therapy and bismuth-containing quadruple regimen for Helicobacter pylori infection

A comparative study of optional dule therapy and bismuth-containing quadruple regimen for Helicobacter pylori infection

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-15007306
Enrollment
Unknown
Registered
2015-10-27
Start date
2015-11-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

diseases of upper digestive tract

Interventions

group A:rabeprazole10mg qid+amoxicillin 750mg qid 14days
group B:rabeprazole 20mg qid+amoxicillin 750mg qid 14days
group C:rabeprazole 20mg bid+bismuth 220mg bid+ Amoxicillin 1g bid+clarithromycin 500mg bid 14days

Sponsors

Daping Hospital, the Third Military Medical University, Chongqing, China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18-70 years old, male or female; 2. 13C breath test positive or the result of rapid ureas test above ++; 3. Endoscopy diagnosed chronic gastritis, uncomplicated duodenal ulcer patients, relatives of patients with gastric or request a healer; 4. Signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Using antibiotics, bismuth, probiotics, H2 receptor antagonists, PPI and drugs metaboliced through the cytochrome P450 2C19 Within four weeks before treatment; 2. Pregnant or lactating women; 3. Patients are also taking non-steroidal anti-inflammatory drugs, adrenocorticotro or alcohol; 4. the presence of other study evaluated the impact of this serious disease such as severe liver disease, heart disease, kidney disease, cancer and other diseases; 5. used in this study for patients with drug allergy; 6. gastrectomy patients or gastric mucosa with high-grade intraepithelial neoplasia; 7. Participated in studies of other drugs before using this study medication within three months; 8. Other factors that were difficult to complete the follow-up or affecting compliance.

Design outcomes

Primary

MeasureTime frame
Eradication rate;

Secondary

MeasureTime frame
Adverse Effects Rate;The patient's compliance;

Countries

China

Contacts

Public ContactChunhui Lan
tiandaochouqin99@hotmail.com+86 13896067955

Outcome results

None listed

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