Actively Recruiting
Evaluation of Dental and Periodontal Health After IPR in Patients in Orthodontic Treatment With Clear Aligners
Led by University of Campania Luigi Vanvitelli · Updated on 2024-11-14
30
Participants Needed
1
Research Sites
75 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Evaluation of Dental and Periodontal Health After IPR in Patients in Orthodontic Treatment With Clear Aligners
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Currently in orthodontic treatment with clear aligners requiring interproximal enamel reduction
- Have permanent teeth
- Have good oral and periodontal health
You will not qualify if you...
- Have enamel defects
- Have cervical caries
- Have periodontal disease
- Have history of trauma or craniofacial anomalies
- Are pregnant
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Multidisciplinary department of Medical-Surgical and Dental Specialties
Naples, Italy, 80138
Actively Recruiting
Research Team
V
Vincenzo Grassia, DDs,PhD
CONTACT
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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