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Analysis of the Efficacy and Safety of the Quadruple Therapy Containing Doxycycline and Bismuth Agents in the Treatment of Helicobacter pylori Infection in Patients with Penicillin Allergy

Analysis of the Efficacy and Safety of the Quadruple Therapy Containing Doxycycline and Bismuth Agents in the Treatment of Helicobacter pylori Infection in Patients with Penicillin Allergy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102564
Enrollment
Unknown
Registered
2025-05-16
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-05-19

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

Conditions

Helicobacter pylori infection

Interventions

Group A:Esomeprazole 20 mg bid, doxycycline 0.1 g bid, metronidazole 0.4 g tid, potassium bismuth citrate 220 mg bid, treatment course 14 days.
Group B:Venlafaxine 20mg twice daily, Doxycycline 0.1g twice daily, Metronidazole 0.4g three times daily, Potassium Citrate 220mg twice daily for a course of 14 days.
Group C:Esomeprazole 20 mg bid, Clarithromycin 0.5g bid, Metronidazole 0.4g tid, Potassium bismuth citrate 220mg bid, treatment course 14 days.

Sponsors

Tianjin Fourth Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Positive Hp infection confirmed by 13C or 14Cbreath test 2. Age 18-70 years; 3. Positive penicillin skin test 4. Previous allergy history to penicillin or amoxicillin. 5. Initial treatment of patients

Exclusion criteria

Exclusion criteria: 1. Those who have used antibiotics, bismuth agents or non-steroidal anti-inflammatory drugs within one month; those who have used acid inhibitors within two weeks before HP eradication therapy; 2. Active peptic ulcer, accompanied by complications such as bleeding, perforation, obstruction and canceration; 3. History of esophageal or gastrectomy surgery; 4. Suffering from serious underlying diseases (heart, lungs, brain, liver, kidneys, etc.), suffering from malignant tumors or other diseases; 5. Pregnant or lactating women; 6. Participate in other research within three months and be unable to express one's own ideas correctly or cooperate with the researcher.

Design outcomes

Primary

MeasureTime frame
Eradication rate;

Secondary

MeasureTime frame
The incidence of adverse events;Economic benefit;

Countries

China

Contacts

Public ContactZhang Qiuzan

Tianjin Fourth Central Hospital

qiuzan_zh@sina.com+86 138 2078 9605

Outcome results

None listed

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