Actively Recruiting

Phase Not Applicable
Age: 17Years - 100Years
All Genders
Healthy Volunteers
ID06685016

Evaluation of Dental and Periodontal Health After Interproximal Enamel Reduction in Orthodontic Treatment With Clear Aligners and Comparison of Laser Diode Versus Sodium Fluoride for Dentin Hypersensitivity

Led by University of Campania Luigi Vanvitelli · Updated on 2024-11-14

30

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate dental and periodontal health after interproximal enamel reduction (IPR) in patients undergoing orthodontic treatment with clear aligners. It compares the effects of Laser diode treatment and sodium fluoride on dentin hypersensitivity, a common discomfort during orthodontic care. The study investigates whether these treatments reduce dentin hypersensitivity better than no treatment in this population. Participants are divided into three groups: one receiving no treatment, one treated with Laser diode, and one receiving sodium fluoride gel. IPR is performed to reduce tooth size and manage crowding or tooth shape issues during orthodontic care. The study observes the impact of these treatments over a period of 3 to 4 months after IPR. During the study, dentin hypersensitivity and periodontal health are assessed before and after IPR at 1 week, 1 month, and 3 months using diagnostic tests like the Visual Analog Scale (VAS). Researchers monitor changes in sensitivity and periodontal indices to measure treatment effects. The total participation involves regular evaluations to track dental health and sensitivity changes throughout the study period.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 17Years - 100Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Currently undergoing orthodontic treatment with clear aligners requiring interproximal enamel reduction
  • Permanent teeth present
  • Good oral and periodontal health
Not Eligible

You will not qualify if you...

  • Having enamel defects
  • Presence of cervical caries
  • Diagnosis of periodontal disease
  • History of trauma or craniofacial anomalies
  • Pregnancy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 3 to 4 months

Participants undergo interproximal enamel reduction (IPR) as part of their orthodontic treatment with clear aligners and are randomly assigned to receive either no treatment, laser diode treatment, or sodium fluoride gel treatment for dentin hypersensitivity.

Visits at baseline (before IPR), immediately after IPR, and at 1 week, 1 month, and 3 months post-IPR

Trial Site Locations

Total: 1 location

1

Multidisciplinary department of Medical-Surgical and Dental Specialties

Naples, Italy, 80138

Actively Recruiting

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Research Team

V

Vincenzo Grassia, DDs,PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

SEQUENTIAL

Primary Purpose

TREATMENT

Number of Arms

3

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Published Research Related To This Trial

Pathogenesis, diagnosis and management of dentin hypersensitivity: an evidence-based overview for dental practitioners.

Xiu-Xin Liu, Howard C Tenenbaum, Rebecca S Wilder...

https://pubmed.ncbi.nlm.nih.gov/32762733