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Clinical Trials/NCT01782079
NCT01782079
Completed
Not Applicable

Assessment of Probiotic Lactobacillus Brevis CD2 Strain Persistence in Oral Cavity. A Pilot Study

University of Roma La Sapienza1 site in 1 country12 target enrollmentStarted: January 2013Last updated:
ConditionsOral Health

Overview

Phase
Not Applicable
Status
Completed
Sponsor
University of Roma La Sapienza
Enrollment
12
Locations
1
Primary Endpoint
Quantification and persistency of Lactobacillus brevis CD2 after oral administration

Overview

Brief Summary

The aim of this study is to select the optimal conditions for quantification in the oral cavity of Lactobacillus brevis CD2, a probiotic strain contained in a commercially available dietary supplement and to assess its persistency after oral administration. Different sets of primers for L. brevis detection will be tested in real-time PCR reactions to find optimal amplification efficiency and target specificity. Primers ability in the identification of L. brevis DNA will be assessed in a pilot study conducted on 12 healthy volunteers clinically free of oral pathologies. The subjects will take 3 tablets/day for 3 days and one tablet on the 4th day. Clinical samples (dorsal surface of tongue, first molar, vestibular fornix and saliva) will be collected at baseline (before beginning the trial), at T0 (in the morning before the assumption of the last tablet) and 3, 6, and 9 hours after taking the last tablet. The quantities of L. brevis DNA will be compared to the total number of bacteria present in the samples. The activity of the enzyme arginine deiminase, responsible for oral pH homeostasis (particularly abundant in the CD2 strain) will be also assessed in the saliva samples before and after treatment, by HPLC measurements.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Basic Science
Masking
None

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Age \> 18 years
  • Healthy subjects with no oral cavity pathologies
  • Written informed consent

Exclusion Criteria

  • Patients with oral diseases
  • Patients with systemic diseases
  • Celiac patients or subjects affected by allergic reactions to soy proteins
  • Use of antibiotics or other probiotics

Outcomes

Primary Outcomes

Quantification and persistency of Lactobacillus brevis CD2 after oral administration

Time Frame: 4 days

Mucosal surface colonization in various mouth sites will be assessed by measuring the number of bacteria by Real Time PCR. Quantities of L. brevis DNA will be compared to the total number of bacteria present in the samples.

Secondary Outcomes

  • Arginine deiminase activity(4 days)

Investigators

Sponsor
University of Roma La Sapienza
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Luciana Mosca, PhD

Principal Investigator

University of Roma La Sapienza

Study Sites (1)

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