Clinical Trials Directory

Trials / Terminated

TerminatedNCT03925818

Low Dose Bismuth Versus Lactobacillus Reuteri for H. Pylori Eradication

Twice-a-day PPI, Tetracycline, Metronidazolequadruple Therapy With Pylera® or Lactobacillus Reuteri for Treatment naïve or for Retreatment of H. Pylori: Two Randomized Pilot Studies

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
99 (actual)
Sponsor
Università degli Studi di Sassari · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study investigates the efficacy of a b.i.d. quadruple therapy containing Pylera® or L. reuteri for H. pylori infection.

Detailed description

Bismuth, metronidazole and tetracycline yielded high cure rates for H. pylori infection. Earlier studies suggested that the bismuth quadruple therapy may be effective when given twice-a-day rather than q.i.d. and that b.i.d. therapy was associated with fewer side effects. The addition of the probiotic Lactobacillus reuteri (Gastrus®) to Lactobacillus reuteri (Gastrus®) that has been shown to increase the cure rates by 10-14%. In another study bismuth supplementation with L. reuteri DSM 17938, in a modified low dose quadruple therapy provided good eradication rates (93.3%; 95% CI : 85-99%) in clinical practice.

Conditions

Interventions

TypeNameDescription
DRUGBismuth Subcitrate PotassiumPylera capsules
DIETARY_SUPPLEMENTGastrusGastrus 1 tablet

Timeline

Start date
2017-08-29
Primary completion
2018-11-29
Completion
2018-12-23
First posted
2019-04-24
Last updated
2019-04-26

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT03925818. Inclusion in this directory is not an endorsement.