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Helicobacter Pylori Rescue Treatment in Patients Allergic to Penicillin

Helicobacter Pylori Rescue Treatment Containing Tetracycline in Patients Allergic to Penicillin:a Prospective Randomized Controlled Study

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05135182
Enrollment
170
Registered
2021-11-26
Start date
2021-11-28
Completion date
2022-12-31
Last updated
2021-11-30

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

Conditions

Helicobacter Pylori Infection

Keywords

Helicobacter pylori, Eradication, Allergic, Penicillin, Tetracycline

Brief summary

The purpose of this study is to assess and compare the effectiveness of furazolidone-tetracycline-containing and metronidazole-tetracycline-containing quadruple regimens for the rescue treatment of Helicobacter pylori infection inpatients allergic to penicillin.

Detailed description

Helicobacter pylori(H.pylori), which infects about 50% of the global population,has been recognized as a main risk factor of multiple gastric pathologies,especially non-cardiac gastric cancer. Strongly evidence supports that H.pylori eradication is an effective approach to reduce the incidence of those pathologies.However,Helicobacter pylori eradication is a challenge in patients allergic to penicillin. Therefore, the investigators aim to assess and compare the effectiveness of furazolidone-tetracycline-containing and metronidazole-tetracycline-containing quadruple regimens for the rescue treatment of Helicobacter pylori infection in patients allergic to penicillin.

Interventions

Furazolidone-tetracycline-containing quadruple regimens

DRUGMetronidazole

metronidazole-tetracycline-containing quadruple regimens

Sponsors

Shandong University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Patients aged 18-70 with H. pylori infection. * Patients with previous Helicobacter pylori eradication. * Patients Allergic to Penicillin.

Exclusion criteria

* Patients treated with H2-receptor antagonist, PPI, bismuth and antibiotics in the previous 4 weeks. * Patients with gastrectomy, acute GI bleeding and advanced gastric cancer. * Patients with known or suspected allergy to study medications. * Currently pregnant or lactating. * Inability to provide informed consent and other situations that could interfere with the examination or therapeutic protocol.

Design outcomes

Primary

MeasureTime frameDescription
Eradication rates in 2 groups12 monthsBoth intention to treat(ITT) and per-protocol(PP) analyses will be used for the assessment of the eradication rates of Helicobacter pylori infections in two groups.

Countries

China

Contacts

Primary ContactXiuli Zuo, MD,PhD
zuoxiuli@sina.com15588818685
Backup ContactXiuli Zuo
zuoxiuli@sina.com15588818685

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026