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Clinical Trials/NCT02705456
NCT02705456
Completed
Not Applicable

Enamel Caries in Orthodontic Patients

Wuerzburg University Hospital1 site in 1 country150 target enrollmentOctober 2014
ConditionsDental Caries

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Dental Caries
Sponsor
Wuerzburg University Hospital
Enrollment
150
Locations
1
Primary Endpoint
Number of developing enamel caries lesions
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

This randomized double-blind two arm controlled clinical trials evaluates the hypothesis that the regular use of a tooth paste containing microcrystalline hydroxylapatite provides a caries preventive effect in caries-susceptible individuals undergoing orthodontic therapy with fixed appliances which is comparable to the caries preventive effect provided by the regular use of a fluoridated tooth paste.

Detailed Description

Introduction According to the criteria of evidence based medicine the use of fluoridated tooth paste as well as fluoridated mouth rinses are,with the exception of dietary control, the only proven measures for the prevention of dental caries. Aim, Study Hypothesis The aim of this randomized double-blind, two arm, controlled clinical trial is evaluation of the hypothesis that the regular use of a tooth paste containing microcrystalline particles of hydroxylapatite in caries-active subjects under orthodontic therapy with fixed appliances will provide at least a comparable extent of caries prevention as the regular use of fluoridated tooth paste during an observation period of 6 months. Material and Methods Study subjects will be recruited from juveniles and young adults, age 12-25, displaying high (≥105 CFU) salivary counts of caries promoting mutans streptococci and seeking orthodontic therapy with fixed appliances. Evaluated parameters are the presence of enamel caries on the buccal aspects of teeth 15-25 according to the criteria of the International Caries Detection and Assessment System (ICDAS), the presence of gingival inflammation assessed by the Gingival Index (GI) the presence of microbial plaque on the evaluated teeth assessed by the Plaque Index (PlI) and the extent of mutans streptococci colonization (MS) on the evaluated teeth and in saliva using standardized cultivation techniques. Primary endpoint of the study is the number and severity of enamel caries lesions according to the ICDAS classification. Exclusion criteria are the presence of ICDAS lesion ≥ 3 on the buccal surfaces of teeth 15-25, the presence of gingival lesions \> GI 2 and the regular use of salivary flow-reducing medications. At baseline, ICDAS scores, as well as GI, PlI and MS will be recorded followed by the incorporation of the fixed orthodontic appliances. Subsequently, using a random list participants are provided with a standardized electric tooth brush and a supply of one of the two experimental tooth pastes (hydroxylapatite(HA)/fluoride (FL)) to be used 2 x daily for the next 6 months. HA-tooth paste contains no fluoride, FL-tooth paste contains stannous fluoride and amine fluoride. At days 28, 84 and 168 (end of study) ICDAS, GI, PlI and MS are recorded again. Additionally all study participants will receive a full mouth preventive professional supragingival tooth cleaning followed by the application of a 1% chlorhexidine gel on all tooth surfaces once every 4 weeks during the course of the trial.

Registry
clinicaltrials.gov
Start Date
October 2014
End Date
December 2016
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Prof. Dr. Ulrich Schlagenhauf

Chairman Dept. of Periodontology

Wuerzburg University Hospital

Eligibility Criteria

Inclusion Criteria

  • Healthy juveniles and young adults with caries-promoting mutans streptococci colonization seeking orthodontic therapy with fixed orthodontic appliances

Exclusion Criteria

  • Oral ulcers
  • Caries lesions on the buccal aspects of teeth 15-25
  • Unrestored caries on any tooth
  • Regular use of medications interfering with salivary flow and/or gingival inflammation

Outcomes

Primary Outcomes

Number of developing enamel caries lesions

Time Frame: 168 days (24 weeks)

Recording of newly developing enamel caries lesions according to the International Caries Detection and Assessment System (ICDAS)

Secondary Outcomes

  • Plaque Coverage using the Plaque Index(168 days (24 weeks))
  • Gingival Inflammation using the Gingival Index(168 days (24 weeks))
  • Mutans Streptococci Colonization(168 days (24 weeks))

Study Sites (1)

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