Association of a probiotic to a Helicobacter pylori eradication scheme does not increase eradication rate neither decrease the adverse events

Completed

• Conditions: Peptic ulcer, functional dyspepsia; Digestive System; Peptic ulcer

• Registration Number: ISRCTN04714018
• Lead Sponsor: Hospital Clinic of the School of Medicine of the University of São Paulo (Brazil)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2011-01-31
• Last Update Posted: 13 January 2015

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 77

Inclusion Criteria

1. Peptic ulcer disease or functional dyspepsia
2. H. pylori infected status was determined by concordance of the at least two biopsy-based diagnostic tests (rapid urease test, histology or 14C labeled urea breath test)
3. Aged 18 to 70 years, either sex

Exclusion Criteria

Previously treated Helicobacter pylori infection

Study & Design

• Study Type: Interventional
• Study Design: Not specified