Surgical wounds
Conditions
Interventions
The 24 patients will be submit the surgical procedure to remove the free gingival graft. After the insertion of the graft on the the recipient site, the patients will be randomly allocated in one of t
Test Group (GT): The wound will be covered with acrylic plate associated with natural latex membrane.
Procedure/surgery
Sponsors
Faculdade de Odontologia de Araraquara- Universidade Estadual Paulista
Faculdade de Odontologia de Araraquara- Universidade Estadual Paulista
Eligibility
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Age between 18 and 60 years old; Presence of less than 2 mm of keratinized gingiva associated with teeth with association of a shallow vestibule or high insertion of a brides in the vestibular region of lower incisors; Present inadequate oral hygiene in the region or report of hygiene difficulty; Probing depht up to 3mm; Class I or II gingival recessions (Miller, 1985); Present good systemic health.
Exclusion criteria
Exclusion criteria: Smokers and former smokers; Diabetics; Presence of chronic or aggressive periodontitis; Patients who use medicinal products that alter the connective tissue metabolism; Patients who were chronically anti-inflammatories and antibiotics users; Bruxism; Ethilics; Chemical dependents; Pregnant; History of radiotherapy in the head and neck region.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected the total closure the surgical wound within 15 days for both groups. Latex membrane will be considered superior to the control treatment if the lesion closes 20% higher than the control treatment in the periods of 3 or 7 days. This parameters will be evaluate by clinical and photographic analysis. These analysis will be perform after 3, 7, 15, and 30 days of the surgery. | — |
Secondary
| Measure | Time frame |
|---|---|
| The treatment with the latex membrane will be considered superior to the control if there is reduction of the pain sensation during the healing phase. This parameter will be evaluate by the use of a VAS scale. This analysis will be perform after 3, 7, 15, and 30 days of the surgery. | — |
Countries
Brazil
Contacts
Public ContactElcio;Guilherme Marcantonio Junior;Oliveira
Faculdade de Odontologia de Araraquara-Unesp;Faculdade de Odontologia de Araraquara-Unesp
Outcome results
None listed