RecruitingNot Applicable

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

Italy30 participantsStarted 2023-06-24

Plain-language summary

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.

Who can participate

Age range17 Years – 100 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * to be in orthodontic treatment with clear aligners and this treatment requires interproximal enamel reduction; * permanent dentition; * good oral and periodontal health. Exclusion Criteria: * enamel defects; * cervical caries; * periodontal disease; * history of trauma or craniofacial anomalies; * pregnancy.

What they're measuring

Assestment of DH after IPR

Timeframe: from 3 to 4 months

Reduction of the Dentin Hypersensitivity

Timeframe: from 3 to 4 months

Trial details

NCT IDNCT06685016

SponsorUniversity of Campania Luigi Vanvitelli

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-12

Contact for this trial

Vincenzo Grassia, DDs,PhD

+39 0815665524 vincenzo.grassia@unicampania.it

View on ClinicalTrials.gov More Dentinal Hypersensitivity trials