Gingival recession
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Volunteers with unitary shallow gingival recessions (less than 4mm), unilateral, type 1 (RT1), in upper or lower canines or premolars; with clinically healthy periodontium and no radiographic bone loss; both sexes; aged between 18 to 55 years.
Exclusion criteria
Exclusion criteria: Volunteers using orthodontic appliances; smokers; pregnant or infants; with previous history of mucogingival or periodontal surgery, fixed or removable prosthodontics, dental cavities, pulp pathology or severe malocclusion involving teeth with gingival recession to be chosen for the study; medication users and/or patients with systemic diseases that may interfere with healing or periodontal health.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Percentage of root coverage over a two-year interval, verified by the method of measuring residual gingival recession of treated teeth, in millimeters and subsequently converted into a percentage, to observe which surgical technique obtained the best result. | — |
Secondary
| Measure | Time frame |
|---|---|
| Decrease in gingival recession in the interval of two years after treatment, verified using the measurement method in millimeters.;Increase in the keratinized tissue width two years after treatment, verified using the measurement method in millimeters.;Decrease in the clinical attachment loss in the interval of two years, verified by the method of measuring the clinical attachment level, in millimeters. ;Increase of gingival thickness within two years after treatment, verified by the measurement method in millimeters. | — |
Countries
Brazil
Contacts
Universidade Federal do Rio Grande do Norte