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Analysis of the therapeutic effect and behavioral improvement of fucoidan on Helicobacter pylori infected college students

Analysis of the therapeutic effect and behavioral improvement of fucoidan on Helicobacter pylori infected college students

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101781
Enrollment
Unknown
Registered
2025-04-29
Start date
2025-05-06
Completion date
Unknown
Last updated
2025-05-05

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 C: Healthy blank control group
Group A:Standard bismuth quadruple therapy, 2week
Group B :High dose group of fucoidan,2g/d,6week
Group D:Standard bismuth quadruple therapy 2week and fucoidan 2g/d 6week
Group E:Standard bismuth quadruple therapy 2week and probiotics 4week

Sponsors

Jilin Medical University, Affililated Hospital of Jilin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 25 Years

Inclusion criteria

Inclusion criteria: 1.Age: 18-25 years old 2.Gender: Male or female, with equal proportions 3.Hp detection: 14C urea breathing test, DPM value >= 100 indicates the presence of Hp infection and requires anti Hp treatment. 4.Life history: No smoking or alcohol abuse history, normal lifestyle and dietary habits during treatment 5.Voluntarily participate in the study and sign an informed consent form 6.Drug history: Within 2 months prior to the first specimen collection, no antibiotics, probiotics, or various drugs that inhibit gastric acid secretion were taken; No history of eradicating Hp treatment

Exclusion criteria

Exclusion criteria: 1.Previous history of Hp eradication 2.Previous history of gastric surgery 3.Have used antibiotics, anti gastric acid secretion drugs, bismuth supplements, probiotics or been allergic to any of the above drugs within 8 weeks 4.Subjects currently participating in clinical studies of other drugs

Design outcomes

Primary

MeasureTime frame
14C UBT DPM value;SCL-90 psychological health score;Gastrointestinal symptoms score;

Secondary

MeasureTime frame
serum inflammatory factors; gut microbiota;

Countries

China

Contacts

Public ContactShi Mai

Jilin Medical University,Affililated Hospital of Jilin Medical University

shimai2003@163.com+86 134 3999 2349

Outcome results

None listed

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