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The Situation of Re-infection of Helicobacter Pylori After Successful Eradication

The Situation of Re-infection of Helicobacter Pylori After Successful Eradication

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04029493
Enrollment
1800
Registered
2019-07-23
Start date
2018-09-01
Completion date
2021-09-30
Last updated
2019-07-23

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

Conditions

Helicobacter Pylori

Keywords

Re-infection

Brief summary

The patients who accept the quadruple eradication program of the helicobacter pylori and success to eradicate helicobacter pylori will be followed-up to observe the situation of re-infection of helicobacter pylori.

Detailed description

The patients with helicobacter pylori accepted he quadruple eradication program of the helicobacter pylori.They will be followed-up from 1 year to 5 years to observe the situation of re-infection of helicobacter pylori.The rate of the re-infection will be described by frequency and percentage.

Interventions

None listed

Sponsors

Shandong University
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years

Inclusion criteria

* Patients, aged between 18 and 70 years old, with positive H. pylori infection that was not eradicated by previous therapies are included. The H. pylori infection is confirmed by the positive rapid urease test or 13C-breath test.

Exclusion criteria

* Patients with significant underlying disease including liver, cardiac, pulmonary, and renal diseases, neoplasia, coagulopathy and genetic diseases, history of gastric surgery, pregnancy, breast-feeding, active gastrointestinal bleeding, the use of PPI, NSAID or antibiotics during the 4 weeks prior to enrolment, and previous history of allergic reactions to any of the medications used in this protocol. Patients previously treated with H. pylori eradication regimens or those unwilling to participate in the study were also excluded.

Design outcomes

Primary

MeasureTime frameDescription
The rate of re-infection4 yearsThe rate of re-infection will be described by the frequency and percentage.

Secondary

MeasureTime frameDescription
The influence factors of the rate of re-infection4 yearsThe chi-square test will be used to compare the influence factors of the rate of re-infection.

Countries

China

Contacts

Primary ContactXiuli Zuo, MD,PhD
zuoxiuli@sina.com15588818685
Backup ContactTian Ma, MD
matian1002@163.com18769781098

Outcome results

None listed

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