An Evaluation of Protective Effects of OpalSeal™ Against Early Dental Decay in Orthodontic Patients
Cavities of Teeth
About this trial
This is an interventional prevention trial for Cavities of Teeth
Eligibility Criteria
Inclusion Criteria:
- Patients age 10 and older seeking treatment at the VCU Orthodontics Clinic who require extraction of at least 2 teeth for orthodontic purposes
- Such teeth should be free of any developmental defects
Exclusion Criteria:
- Patients under 10 years of age
- Patients with defective teeth
- Those who cannot provide consent/assent OR not able to follow research protocols
- Protected population (prisoners)
Sites / Locations
- School of Dentistry, Virginia Commonwealth University
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
OpalSeal
Transbond XT
OpalSeal will be applied to the buccal surfaces of to-be-extracted teeth on one side of the mouth which will be determined randomly for each participant during bonding of orthodontic brackets, or to the proximal surfaces following IPR in accordance to manufacturer instructions. Since OpalSeal has fluoride releasing capability, this would be experimental arm
TransbondXT will be applied to the buccal surfaces of to-be-extracted teeth on the other side of the mouth which will be determined based on which side received OpalSeal for each participant during bonding of orthodontic brackets, or to the proximal surfaces following IPR in accordance to manufacturer instructions. Transbond XT does not have fluoride and hence would be considered as a placebo.