The Effect of Different Adhesion Strategies on the Clinical Success

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age14-75
SponsorIstanbul University

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

Treatment groups

41 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators