Skip to content

Canceled by the investigator Effect of vonoprazan-amoxicillin dual therapy on gut microbiota

Effect of vonoprazan-amoxicillin dual therapy on gut microbiota

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300071812
Enrollment
Unknown
Registered
2023-05-25
Start date
2023-06-01
Completion date
Unknown
Last updated
2023-07-10

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

Conditions

Helicobacter pylori

Interventions

10-day vonoprazan-amoxicillin dual therapy group:10-day vonoprazan-amoxicillin dual therapy
14-day vonoprazan-amoxicillin dual therapy group:14-day vonoprazan-amoxicillin dual therapy

Sponsors

Wenchang People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Age range from 18-70 years old; 2. H. pylori infection diagnosed by C13/ C14-urea breath test; 3. Without digestive diseases except dyspepsia and chronic gastritis, without surgical history, without history of serious cardiovascular,respiratory, endocrine (diabetes), kidney disease, blood disease; ( 4. In recent 3 months, patients without severe diarrhea (watery stool for more than 3 times a day and lasting for more than 3 days), without constipation (defecation less than 2 times a week and accompanied by difficulty defecating), without blood in the stool ; ? Informed and agreed to participate in the study

Exclusion criteria

Exclusion criteria: 1. With a history of H. pylori eradication; 2. Alcohol abuse, illicit drug use or drug addiction, or consumption of >21 units of alcohol per week (6300 mL beer, 525 mL spirits, or 2100mL wine) in the 12 months prior to screening; 3. Taking antibiotics, probiotics, PPI, antiviral/fungal drugs, NSAIDs, mucosal protectants, immunosuppressants or hormones in the past 3 months; 4.Taking laxatives or having acute gastroenteritis in the past 4 weeks; 5. Pregnancy and lactation; 6. Excessive obesity; 7. Allergy to penicillin or other drug in this study; 8. Currently participating in another clinical study; 9. Patients assessed as unsuitable by investigators.

Design outcomes

Primary

MeasureTime frame
Eradication rate;Safety;the change of gut microbiota;

Countries

China

Contacts

Public ContactTingting Xu

Wenchang People's Hospital

452064807@qq.com+86 130 6986 3801

Outcome results

None listed

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