Palete
Conditions
Interventions
This is a randomized, controlled, prospective, split-mouth, double-blind experimental clinical study. Fifteen patients will receive treatment for the surgical wound on the palate produced after the co
D25.339.816.500
D25.919.367
Sponsors
Faculdade São Leopoldo Mandic
Faculdade São Leopoldo Mandic
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: To be 18 or over; do not report the presence of systemic diseases; present healthy periodontium and periodontal stability after conventional periodontal therapy; present a plaque and bleeding index on probing < 10% of sites; needing periodontal plastic surgery using a deephelialized free gingival graft (EGL-d) to treat single and multiple gingival recessions (Class I and II of Cairo, 2011) in the mandible or anterior region of the maxilla (canine to canine); no previous history of palatal graft removal
Exclusion criteria
Exclusion criteria: Pregnancy; report use of medication that may have an adverse effect on periodontal tissues; inadequate endodontic treatment; tooth mobility at the surgery site
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative pain in the region of the palatal surgical wound protected by light-curing fluid composite resin or by cyanoacrylate-based tissue adhesive measured using a VAS questionnaire from 0 to 10 on days 1, 2, 3, 4, 5, 6, 7, 10 and 14. | — |
Secondary
| Measure | Time frame |
|---|---|
| Changes in the color of palatal surgical wounds protected for 7 days with light-polymerizable fluid composite resin or cyanoacrylate-based tissue adhesive verified by matching the preoperative photograph of the region with the postoperative photographs on days 7, 14, 21 and 30.;Changes in the contour of palatal surgical wounds protected for 7 days with light-polymerizable fluid composite resin or cyanoacrylate-based tissue adhesive verified by matching the preoperative photograph of the region with the postoperative photographs on days 7, 14, 21 and 30.;Changes in the tissue texture of palatal surgical wounds protected for 7 days with light-polymerizable fluid composite resin or cyanoacrylate-based tissue adhesive verified by matching the tissue adjacent to the region with postoperative photographs on days 7, 14, 21 and 30. ;Number of analgesics ingested (sodium dipyrone 500mg) during 7 postoperative days in the presence of a palatal surgical wound protected by light-cured fluid composite resin or cyanoacrylate-based tissue adhesive. | — |
Countries
Brazil
Contacts
Public ContactThiago Cedro
Faculdade São Leopoldo Mandic
Outcome results
None listed