Clinical Trials Directory

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UnknownNCT04674774

Efficacy of Tegoprazan Based Bismuth Quadruple Therapy for Helicobacter Pylori Infection

Efficacy of Tegoprazan Based Bismuth Quadruple Therapy Compared With Bismuth Quadruple Therapy for Helicobacter Pylori Infection: Randomized, Double-blind, Active-Controlled Study

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
217 (actual)
Sponsor
Incheon St.Mary's Hospital · Academic / Other
Sex
All
Age
19 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This study aims to investigate eradication rate, drug compliance, and adverse events in patients with confirmed Helicobacter pylori infection between tegoprazan, bismuth, metronidazole, and tetracycline for 14 days (TBMT) and PPI, bismuth, metronidazole, and tetracycline for 14 days (LBMT)

Detailed description

This is a multi-center, double-blind, randomized, active-controlled study.

Conditions

Interventions

TypeNameDescription
DRUGTegoprazanoral administration of tegoprazan-based bismuth quadruple therapy(tegoprazan 50 mg b.i.d, bismuth 300 mg q.i.d, metronidazole 500 mg t.i.d, tetracycline 500 mg q.i.d) for 14 days
DRUGLansoprazoleoral administration of PPI-based bismuth quadruple therapy(lansoprazole 30 mg b.i.d, bismuth 300 mg q.i.d, metronidazole 500 mg t.i.d, tetracycline 500 mg q.i.d) for 14 day

Timeline

Start date
2021-03-04
Primary completion
2022-02-28
Completion
2022-03-31
First posted
2020-12-19
Last updated
2022-02-10

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT04674774. Inclusion in this directory is not an endorsement.