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Xylitol Chewing-gums: Concentration in Saliva and Antibacterial Effect

Xylitol Chewing-gums: Concentration in Saliva and Antibacterial Effect (In-vivo and In-vitro Study)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03971981
Enrollment
32
Registered
2019-06-03
Start date
2018-02-01
Completion date
2019-05-28
Last updated
2019-06-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dental Caries, Periodontal Diseases

Keywords

Xylitol, Saliva, Bacteria, Dental Plaque, Antimicrobial effect, Chewing gum

Brief summary

a double-blind cross-over in vivo study was performed to measure the salivary concentration of Xylitol released from the two chewing gums containing different amount of the polyol. The study had a cross-over design: the first half of the sample used the chewing-gum with Xylitol as the only sweeteners (64.5% of chewing-gum weight) and the other half use the chewing-gum with Xylitol among the sweeteners (22% of chewing-gum weight), after a 7-days wash-out period, the two sub-groups inverted the chewing gums. Subjects were instructed to consume the products as they normally would be consumed.

Detailed description

x

Interventions

DIETARY_SUPPLEMENT100% Xylitol Gum

Subjects were instructed to consume the gums as they normally would be consumed.

DIETARY_SUPPLEMENT22% Xylitol Gum

Subjects were instructed to consume the gums as they normally would be consumed.

Sponsors

University of Milan
CollaboratorOTHER
Università degli Studi di Sassari
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Intervention model description

a double-blind cross-over in vivo study was performed to measure the salivary concentration of Xylitol released from the two chewing gums containing different amount of the polyol. The study had a cross-over design: the first half of the sample used the chewing-gum with Xylitol as the only sweeteners (64.5% of chewing-gum weight) and the other half use the chewing-gum with Xylitol among the sweeteners (22% of chewing-gum weight), after a 7-days wash-out period, the two sub-groups inverted the chewing gums. Subjects were instructed to consume the products as they normally would be consumed.

Eligibility

Sex/Gender
ALL
Age
19 Years to 26 Years
Healthy volunteers
Yes

Inclusion criteria

* good general health, * the absence of diseases that can alter the saliva secretion rate * a stimulated saliva flow at least of 1 ml/min.

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
Change of Salivary concentration of Xylitol9 daysXylitol concentration using spectrophotometer analysis was determined in saliva before, at 0.30, 1.00, 2.00, 5.00, 10.00 minutes using the chewing-gum, and after the gum discarded at 15.00, 20.00 and 25.00 minutes.

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026