Clinical Trials Directory

Trials / Completed

CompletedNCT06561711

Optimization of Minocycline for Helicobacter Pylori Rescue Treatment

Optimization of Minocycline-containing Bismuth Quadruple Therapy for Helicobacter Pylori Rescue Treatment: a Multicentre, Randomized Controlled Trial

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
480 (actual)
Sponsor
Shanghai Jiao Tong University School of Medicine · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The efficacy of bismuth-containing quadruple therapy with minocycline and metronidazole was not inferior to classical bismuth quadruple therapy for refractory H. pylori infection, though also accompanied with high occurrence of adverse events (55.4%). Optimization of minocycline-based regimen to achieve high eradication rate with fewer adverse events is imperative. This study aimed to compare the efficacy and tolerability of a 14-day bismuth-containing quadruple rescue therapy with different dosage of minocycline and metronidazole compared to classical bismuth quadruple therapy.

Conditions

Interventions

TypeNameDescription
DRUGVonoprazanPotassium competitive acid blocker
DRUGBismuth Potassium CitrateGastric mucosal protective drug with anti-H. pylori effect
DRUGTetracycline,MetronidazoleAntibiotics for H. pylori eradication
DRUGMinocycline,MetronidazoleAntibiotics for H. pylori eradication

Timeline

Start date
2024-08-21
Primary completion
2026-02-21
Completion
2026-02-21
First posted
2024-08-20
Last updated
2026-03-25

Locations

4 sites across 1 country: China

Source: ClinicalTrials.gov record NCT06561711. Inclusion in this directory is not an endorsement.

Optimization of Minocycline for Helicobacter Pylori Rescue Treatment (NCT06561711) · Clinical Trials Directory