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Trials / Enrolling By Invitation

Enrolling By InvitationNCT07142798

to Assess the Eradication Rate of 14-day Bismuth/Amoxicillin/PCAB Triple Therapy for the Treatment of Helicobacter Pylori Infection

Efficacy of Bismuth/Amoxicillin/Potassium-competitive Acid Blocker Triple Therapy for the Treatment of Helicobacter Pylori Infection in Taiwan

Status
Enrolling By Invitation
Phase
N/A
Study type
Interventional
Enrollment
200 (estimated)
Sponsor
Kaohsiung Medical University · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

To assess the efficacy and safety of 14-day bismuth/amoxicillin/PCAB triple therapy for the treatment of Helicobacter pylori infection in Taiwan

Conditions

Interventions

TypeNameDescription
DRUGBismuth amoxilillin potassiumvonoprazan 20mg, Twice a day amoxicillin 750mg,Four times a day tripotassium dicitrate bismuthate 300mg,Four times a day for 14 days

Timeline

Start date
2024-09-26
Primary completion
2025-12-31
Completion
2026-01-31
First posted
2025-08-27
Last updated
2025-08-27

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT07142798. Inclusion in this directory is not an endorsement.