| Literature DB >> 21170011 |
Abstract
DESIGN: This was a randomised clinical trial (note that the initial screening used a cluster randomised in part design). INTERVENTION: A total of 176 children (7-9 years old) with high MS scores were randomised into equal groups. For 6 months the xylitol group chewed five times during the day, 11.6 grams of a mixed gum containing 36.6% xylitol and other polyols (34.5%). while the control group chewed an identical dose of a non xylitol gum sweetened with a mixture of different polyols (71.1%). OUTCOME MEASURE: At baseline, 3 months, 6 months and 9 months (3 months after chewing) children were assessed for both plaque acidogenicity (after sucrose challenge) and salivary MS.Entities:
Year: 2010 PMID: 21170011 DOI: 10.1038/sj.ebd.6400755
Source DB: PubMed Journal: Evid Based Dent ISSN: 1462-0049