Clinical Trials Directory

Trials / Completed

CompletedNCT02036151

Impact of Maternal Xylitol Consumption on Mutans Sterptococci

Impact of Maternal Xylitol Consumption on Mutans Sterptococci ,Plaque and Caries Levels in Children

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
60 (actual)
Sponsor
King Abdulaziz University · Academic / Other
Sex
All
Age
10 Months – 36 Months
Healthy volunteers
Accepted

Summary

The study was designed to determine whether maternal xylitol consumption through regular chewing of xylitol gums can affect the salivary mutans streptococci (MS), dental caries, and dental plaque levels of their children.

Detailed description

Method: Study sample included 60 mother and child pairs with high salivary mutans streptococcus (MS) levels. Samples were randomly divided into experimental group (30 pairs) and control group (30 pairs). Mothers in the experimental group received xylitol chewing gum treatment three times/day for three months, whereas the controls received fluoride varnish. Both groups received oral hygiene instructions, dietary counseling and restorative treatment. All children were examined after 6, 12 and 18 months from the initiation of the study to assess caries, plaque and salivary mutans streptococcus (MS) levels.

Conditions

Interventions

TypeNameDescription
DRUGxylitolMothers in the experimental group were instructed to chew 1 pellet of xylitol gum (Fennobon Oy, Yrittäjäntie, Finneland -gum, 3 times ) for a period of 3 months. control mothers did not receive any medications. All mothers received oral hygiene instructions and restorative treatment when needed. Offspring of both the experimental and control groups did not receive any medication and were followed for at 6,12, 18 and 24 month from initiation of mothers consumption. month
DRUGfluoride varnish applicationThe control group participated in a preventive program under the supervision of the Pediatric Dentistry Department. The program activities consisted of oral hygiene instructions, fluoride varnish application (Duraphat 5% Na F ,Ultradent Products, Utah, USA) and restorative treatment when needed.

Timeline

Start date
2009-02-01
Primary completion
2011-07-01
Completion
2011-09-01
First posted
2014-01-14
Last updated
2014-01-14

Locations

1 site across 1 country: Saudi Arabia

Source: ClinicalTrials.gov record NCT02036151. Inclusion in this directory is not an endorsement.