Evaluating dental health after enamel reduction in orthodontic patients using clear aligners

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates the dental and periodontal health of patients undergoing orthodontic treatment with clear aligners who require interproximal enamel reduction (IPR). It compares the effects of using a laser diode versus sodium fluoride on dentin hypersensitivity during treatment. The study aims to determine if these interventions can reduce the incidence of dentin hypersensitivity compared to a control group. The methodology involves assessing dental health outcomes and sensitivity levels using a Visual Analog Scale (VAS).

Why it matters

Who can join: the full rules

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.

Where it's running

• Multidisciplinary department of Medical-Surgical and Dental Specialties
  Naples, Italy Recruiting

Study contacts

• Principal investigator: Vincenzo Grassia, DDs,PhD — University of Campania Luigi Vanvitelli
• Study coordinator: Vincenzo Grassia, DDs,PhD
• Email: vincenzo.grassia@unicampania.it
• Phone: +39 0815665524

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.