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Xylitol Adult Caries Trial (X-ACT)

Phase 3
Completed
Conditions
Dental Caries
Interventions
Dietary Supplement: xylitol
Dietary Supplement: inactive lozenge
Registration Number
NCT00393055
Lead Sponsor
University of North Carolina, Chapel Hill
Brief Summary

The purpose of the trial is to determine the extent to which daily use of xylitol lozenges reduces the appearance of new caries lesions in adults who tend to experience such lesions (i.e., caries-active adults).

Detailed Description

Dental caries incidence is higher in adults than children. Recent recommendations from both the Centers for Disease Control and an NIH Consensus Development Conference on dental caries call for clinical trials of caries prevention methods in caries-active adults. Little is known about the effectiveness of caries prevention methods in adults, and virtually no information exists with respect to prevention among adults who are at elevated risk for developing caries lesions. This application describes a clinical trial of an intervention to prevent dental caries in caries-active adults that is responsive to the CDC and Consensus Conference recommendations.

The Xylitol for Adult Caries Trial (X-ACT) is a three-year, multi-center, randomized, placebo-controlled, double-blind study to determine the effectiveness of xylitol lozenges in reducing the incidence of coronal and root caries in caries-active adults. The intervention is the daily use of xylitol lozenges. Participants will be 750 adults (ages 25-75) with current or recent caries lesions who are dental school patients at one of three Clinical Centers in Chapel Hill, NC, Birmingham, AL, and San Antonio TX. These Clinical Centers offer diverse populations with substantial proportions of minority populations that enhance the generalizability of the findings. The Study Chair is located at the University of North Carolina-Chapel Hill, and the Data Coordinating Center is at the Kaiser Permanente Center for Health Research in Portland, OR.

This intervention is being tested because it represents a potentially effective caries prevention method with a high likelihood of adoption by dental practitioners as an "add on" caries preventive method for their caries-active patients. The potential for adoption of the intervention is an important consideration because current data suggest that caries-active adults are underexposed to caries-preventive treatment in dental practices. If effective, the intervention also holds potential as a public health measure.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
709
Inclusion Criteria
  • age 25-80
  • at least one caries lesion in year prior to enrollment
  • at least 12 teeth without crowns
  • no allergies to xylitol or aspartame
  • anticipate remaining in area for 3 years
Read More
Exclusion Criteria
  • 10 or more caries lesions in year prior to enrollment
  • currently receiving long-term antibiotic therapy
  • history of head and neck radiation
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
xylitol lozengexylitol1g xylitol lozenge. Five/day, dissolved in mouth
inactive lozengeinactive lozenge1g placebo lozenge. Five/day, dissolved in mouth
Primary Outcome Measures
NameTimeMethod
combined root and coronal D2FS (dental caries) increment3 year
Secondary Outcome Measures
NameTimeMethod
combined root and coronal D12FS (dental caries) incrementthree year
separate root and coronal D12FS (dental caries) increments3 years
association of lozenge use with D12FS (dental caries) in control group only3 years

Trial Locations

Locations (3)

University of Texas Health Science Center

🇺🇸

San Antonio, Texas, United States

University of Alabama at Birmingham

🇺🇸

Birmingham, Alabama, United States

University of North Carolina School of Dentistry

🇺🇸

Chapel Hill,, North Carolina, United States

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