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Construction of Clinical Evaluation Technology Platform for New Drugs of Major Diseases--Exploring New Eradication Treatment Program for Drug-Resistant Helicobacter Pylori

Construction of Clinical Evaluation Technology Platform for New Drugs of Major Diseases--Exploring New Eradication Treatment Program for Drug-Resistant Helicobacter Pylori

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900023228
Enrollment
Unknown
Registered
2019-05-17
Start date
2019-02-01
Completion date
Unknown
Last updated
2019-05-20

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

Conditions

H.pylori infection

Interventions

Minocycline Innovation Test Group:Selective treatment of amoxicillin or furazolidone combined with minocycline
Genetic optimization test group:After high-throughput second-generation sequencing of DNA, optimizing antibiotics based on drug resistance and sensitivity
Classic antibiotic control group:An empirical antibiotic medication that is not a previous option

Sponsors

Beijing Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Aged = 18 years old; (2) Clearly H.pylori infection (13C breath test positive or histopathological staining positive or rapid urease positive); (3) Had received at least 1 H.pylori eradication therapy, but determined that eradication failed; (4) The days of conforming eradication failure is more than 3 months.

Exclusion criteria

Exclusion criteria: (1) Digestive malignant tumors; (2) History of upper gastrointestinal surgery; (3) Antibiotics, proton pump inhibitors, H2 receptor antagonists, and expectorants have been used in the past 4 weeks; (4) There are symptoms that may related to malignant disease, such as gastrointestinal bleeding, persistent vomiting, weight loss, difficulty swallowing, abdominal mass, etc.; (5) Pregnant and lactating women; (6) Combine diseases such as severe heart, brain, lung, kidney and liver dysfunction; (7) Those who are allergic to the drugs used in this study protocol; (8) Those with poor compliance or non-cooperation such as mental symptoms and drug addiction.

Design outcomes

Primary

MeasureTime frame
C13 urea breath test;High-throughput sequencing;

Countries

China

Contacts

Public ContactLuo Qingfeng

Beijing Hospital

luoqf2000@126.com+86 13811519095

Outcome results

None listed

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