Recruitment

Recruitment Status
Not yet recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Dental Caries
  • Dental Plaque
  • Dental White Spot
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: Subjects will be randomized into one of 3 groups, each of which will receive two of the following three interventions: extended contact varnish, traditional fluoride varnish, placebo varnish. Subjects will receive the interventions in a split-mouth design, with one treatment on half of their teeth and another treatment on the other half of their teeth.Masking: Double (Participant, Outcomes Assessor)Masking Description: Participants will not know which interventions they receive. The investigator, who will be providing the treatment, will be aware of which treatments they are receiving (the investigator is impossible to mask due to the different applications of the treatment interventions). Outcomes assessors will be masked and score outcomes based on photos and microbiological data that is de-identified.Primary Purpose: Treatment

Participation Requirements

Age
Between 12 years and 19 years
Gender
Both males and females

Description

Orthodontic patients ages 12-19 (target 120 subjects) nearing the end of treatment with metal braces at the UCLA Orthodontic Clinic will be recruited. Patients will be consented by Dr. Joseph Mullen, or an eligible and trained orthodontic resident. Participants will be assigned into one of three gro...

Orthodontic patients ages 12-19 (target 120 subjects) nearing the end of treatment with metal braces at the UCLA Orthodontic Clinic will be recruited. Patients will be consented by Dr. Joseph Mullen, or an eligible and trained orthodontic resident. Participants will be assigned into one of three groups via stratified permuted block randomization. The groups will receive treatment as follows in a split-mouth study design: Group 1 - extended contact varnish on upper left and lower right teeth, 5% fluoride varnish on upper right and lower left teeth Group 2 - placebo varnish on upper left and lower right teeth, extended contact varnish on upper right and lower left teeth Group 3 - 5% fluoride varnish on upper left and lower right teeth, placebo varnish on upper right and lower left teeth On the day their braces are coming off, each subject will fill out an oral health questionnaire and the investigators will use Trace Plaque Disclosing Liquid (a safe, commercially available product) to visualize the plaque. Intraoral photos of only the teeth surfaces will be taken. Dental plaque samples will be collected from buccal surfaces of the teeth. The plaque will be collected with a sterile dental instrument and carefully deposited into a sterile plastic collection tube containing a nutrient solution for the bacteria. After collection, the samples will be taken to the laboratory for further analysis and no subject identifiers will be used. Total DNA from each will be extracted, and sequencing analysis will be performed in order to determine the relative abundance of each species in the samples. After the subject's braces are removed, a professional cleaning will be done of the subjects teeth to remove all remaining plaque and calculus buildup on the teeth. After the cleaning, the subject will rinse with water and a second set of intraoral photos will be taken. The teeth will then be air dried for 15 seconds, and a third set of intraoral photos will be taken. The extent of the demineralized white spot lesions will be quantitatively assessed using the DiagnoDent, where a light is shined on the teeth and the fluorescence is measured to assess the depth/severity of the demineralization. The study varnishes will be applied to the patient's teeth (according to the manufacturer's instructions), consistent with their group allocation. The patient will be given written post-op instructions, including oral hygiene instructions to use OTC sodium fluoride toothpaste and a manual toothbrush. The subjects will be asked to refrain from using adjunctive fluoride products (such as mouthwash) for the duration of the study. Since all subjects will receive another professional cleaning at their 6-month visit (consistent with the standard of care to receive professional cleanings every 6 months), they will be asked to not receive additional dental cleanings from outside providers. Subjects will return to the clinic after 30, 90, and 180 days. At each appointment, they will have their plaque disclosed with Trace Plaque Disclosing solution, have 3 sets of intraoral photos taken (with plaque, with clean/moist teeth, and with clean/dry teeth), have the white spot lesion severity measured with the DiagnoDent, and have the varnishes reapplied to their teeth. At the final visit (day 180), subjects will receive a professional dental cleaning after the photos have been assessed. After study completion, blinded investigators will use the intraoral photos to (1) assess the extent of plaque using various plaque indices, and (2) assess the severity of white spot lesions using various visual indices.

Tracking Information

NCT #
NCT04528134
Collaborators
Not Provided
Investigators
Principal Investigator: Joseph Mullen, DDS University of California, Los Angeles Study Chair: Renate Lux, PhD University of California, Los Angeles Study Director: Nini Tran, DDS, PhD University of California, Los Angeles