About this trial
The study will involve 41 people who regularly seek treatment at clinics. Participants must be in generally good health and be older than eighteen. must have at least 20 teeth in an occlusion and maintain appropriate dental hygiene. They have to be treated for a minimum of four non-cancerous cervical lesions in their mouths.Four non-carious cervical lesions from patients will be separated into four groups, and adhesive material will be applied to the lesions in each group using different procedures. Evaluation will be performed based on World Dental Federation (FDI) criteria after initial, ½, 1, 2, 3, 4, and 5 years.
Eligibility criteria
Qualifiers
Over the age of 18 years
Good oral hygiene normal occlusal relationship with natural dentition
At least 20 teeth are in occlusion The tooth with the lesion must be vital. non-mobile and non-carious
Accepts Healthy Volunteers
Disqualifiers
Poor oral hygiene poor general health condition
Bruxism or uncontrolled parafunction
Patients with periodontal or gingival diseases
Trial design
Treatments tested in this trial
- Treatment of cervical lesions