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Evaluation of the clinical efficacy of fucoidan in the eradication of Helicobacter pylori

Clinical effect and mechanism of fucoidan on Helicobacter pylori eradication

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081499
Enrollment
Unknown
Registered
2024-03-04
Start date
2024-03-04
Completion date
Unknown
Last updated
2024-03-11

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

Conditions

Helicobacter pylori infection

Interventions

Test group:fucoidin

Sponsors

The Affiliated Hospital of Qingdao University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Age of 18-70 years old, both sexes; (2) Hp infection confirmed by 13C urea breath test within 3 months; (3) no previous HP eradication therapy; (4) According to the investigator's judgment, the subjects could understand all relevant contents of the study and comply with the requirements of the study protocol; (5) The subjects understood and signed the informed consent before the study process was started. (6) agree to take effective contraceptive measures from the time of signing the informed consent until the end of the trial.

Exclusion criteria

Exclusion criteria: (1) Patients who had used antibiotics, bismuth, probiotics or traditional Chinese medicine with antibacterial effects within the past 4 weeks, PPI or P-CAB within 2 weeks, or could not stop using the above drugs during the study; (2) patients had undergone gastric surgery; (3) complicated with gastric cancer and high-grade neoplasia; (4) The subject has any unstable or uncontrolled cardiovascular, pulmonary, hepatic, renal, urogenital, hematological, coagulation, immunological, metabolic, or other medical diseases that the investigator believes will interfere with the study results or endanger the safety of the subject; (5) The subjects had a history of severe allergy (such as drug allergy) to fucoidan, which may affect the safety of the subjects during the study. (6) pregnant or lactating patients or patients who plan to have children in the past 3 months; (7) The subjects had active psychosis, which the researcher thought might interfere with their compliance with the study procedure; (8) subjects were unable to attend all study visits or follow study procedures; (9) have participated or are participating in other clinical research within 3 months.

Design outcomes

Primary

MeasureTime frame
Carbon 13 urea breath test;

Secondary

MeasureTime frame
symptom;

Countries

China

Contacts

Public ContactZibin Tian

The Affiliated Hospital of Qingdao University

tianzbsun@163.com+86 186 6180 5123

Outcome results

None listed

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