Evaluation of Dental and Periodontal Health After IPR in Patients in Orthodontic Treatment With Clear Aligners

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age17-100
SponsorUniversity of Campania Luigi Vanvitelli

About this trial

This study aimed to evaluate dental and periodontal health after interproximal enamel reduction and to compare Laser diode (a device used in the Orthodontic Program) and sodium fluoride (often used in the Orthodontic Program and in the Material Dental Program). The hypothesis was that the intervention groups would show a lower dentin hypersensitivity incidence than the control group during orthodontic treatment.

Eligibility criteria

Qualifiers

to be in orthodontic treatment with clear aligners and this treatment requires interproximal enamel reduction;

permanent dentition;

good oral and periodontal health.

Disqualifiers

enamel defects;

cervical caries;

periodontal disease;

history of trauma or craniofacial anomalies;

Trial design

Treatments tested in this trial

  • Evaluation of Dentin hypersensitivity with VAS scale

Treatment groups

30 Participants
are divided into 3 treatment groups