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Effect and molecular mechanism of bismuth spray under gastroscopy in the treatment of Helicobacter pylori

Effect and molecular mechanism of bismuth spray under gastroscopy in the treatment of Helicobacter pylori

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072600
Enrollment
Unknown
Registered
2023-06-19
Start date
2023-07-01
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

Helicobacter pylori infection

Interventions

Treatment group:Bismuth spray under gastroscope
Control group:Traditional oral medicine

Sponsors

The First Affiliated Hospital of Fujian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: a. Positive rapid urease test and/or urea breath test. b. According to the Sixth National Consensus Report on the Management of Helicobacter pylori Infection, it has indications of Hp eradication. Peptic ulcer, whether active or not and with or without a history of complications; Gastric mucosa-associated lymphoid tissue lymphoma; Early gastric cancer underwent endoscopic submucosal dissection or subtotal gastrectomy. Family history of gastric cancer; Plan to take non-steroidal anti-inflammatory drugs for a long time; Hp gastritis; Gastric hyperplastic polyp; Hp-related dyspepsia; Long-term use of proton pump inhibitors; Iron deficiency anemia of unknown origin; Primary immune thrombocytopenia; Vitamin B12 deficiency; Confirmed Hp infection (no countervailing factor for eradication therapy). c. Age 18 to 70 years old. d. No history of bismuth allergy.

Exclusion criteria

Exclusion criteria: a. Patients who had taken antibiotics or bismuth within 4 weeks before treatment, proton pump inhibitors or H2 receptor antagonists within 2 weeks before treatment, and antiplatelet or anticoagulant drugs within 1 week before treatment. b. Patients whose general condition is not acceptable for gastroscopy. c. Patients with severe heart, kidney, lung and liver diseases. d. Known or suspected allergy to the drug. e. Participants in other clinical trials. f. Other conditions that the researchers deem inappropriate for clinical trials.

Design outcomes

Primary

MeasureTime frame
Urea breath test;

Countries

CChina

Contacts

Public ContactLian Tingting

The First Affiliated Hospital of Fujian Medical University

lttnow@163.com+86 183 4498 8931

Outcome results

None listed

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