Differences in the Eradication of Helicobacter Pylori by Different Therapies
Launched by WANG XIAOYAN · Oct 27, 2021
Trial Information
Current as of April 24, 2025
Unknown status
Keywords
ClinConnect Summary
A single-center, prospective, open-label, parallel control design was conducted to enroll 100 patients with confirmed Helicobacter pylori infection. Patients were randomly divided into four groups, respectively accept four treatment regimens including (1) Vonoprazan Fumarate + amoxicillin + doxycycline, (2) Vonoprazan Fumarate + furazolidone + doxycycline, (3) esomeprazole + colloidal bismuth tartrate + amoxicillin + doxycycline, and (4) esomeprazole + colloidal bismuth tartrate + furazolidone + doxycycline. The effectiveness, safety and compliance of the four regimens were compared, and th...
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Age ≥18 years, ≤80 years
- • 2. Urea breath test (UBT) was positive for Hp infection;
- • 3. WIthout any anti-Hp treatment before
- • 4. Endoscopy was performed within 1 month
- • 5. Understanding the purpose and procedure of the study, voluntarily participating in the study and signing a written informed consent.
- Exclusion Criteria:
- • 1. Allergic to drugs used in this clinical study;
- • 2. Using PPI, histamine H2 receptor antagonist, antibiotics, bismuth, probiotics or drugs with antibacterial effects within 4 weeks before treatment.
- • 3. Using adrenal corticosteroids, non-steroidal anti-inflammatory drugs and anticoagulants
- • 4. The disease or clinical condition that may interfere with the treatment evaluation of the study, such as liver disease, cardiovascular disease, lung disease, kidney disease, metabolic disease, psychiatric disease, or malignant tumor
- • 5. Pregnant or lactating women
- • 6. Participated in other clinical studies within 3 months prior to the registration of this clinical study
- • 7. Suspected history of antibiotic abuse
- • 8. Patients with craniocerebral injury, mental illness or epilepsy who cannot communicate with others or other diseases that may affect follow-up
About Wang Xiaoyan
Wang Xiaoyan is a dedicated clinical trial sponsor committed to advancing medical research and improving patient outcomes through innovative studies. With a focus on rigorous scientific methodologies and ethical standards, the organization collaborates with leading healthcare professionals and institutions to conduct comprehensive clinical trials across various therapeutic areas. Wang Xiaoyan's mission is to bridge the gap between research and clinical practice, ensuring that new treatments are effectively evaluated and made accessible to patients in need. Their expertise in trial design, regulatory compliance, and data management underscores their commitment to excellence in clinical research.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Changsha, Hunan, China
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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