A New Surgical-restorative Approach to Treat Gingival Recessions Associated With Non-carious Cerv… (NCT02817763) | Clinical Trial Compass
CompletedNot Applicable
A New Surgical-restorative Approach to Treat Gingival Recessions Associated With Non-carious Cervical Lesions (NCCL)
40 participantsStarted 2014-02
Plain-language summary
The aim of the present study is to evaluate the clinical, aesthetic and patient-centered parameters of connective tissue graft associated or not with partial resin composite (RC) for the treatment of gingival recession with NCCL, performed before the surgical procedure.
Who can participate
Age range18 Years – 65 Years
SexALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* presenting Miller class I or II gingival recession in the maxillary canines or premolars associated with non-carious cervical lesion;
* teeth included in the study should present pulp vitality;
* patients presenting no signs of active periodontal disease and full-mouth plaque and bleeding score ≤ 20%;
* patients older than 18 years old;
* probing depth Ë‚ 3 mm in the included teeth;
* patients who agreed to participate and signed an informed consent form
Exclusion Criteria:
* patients with systemic problems (cardiovascular, blood dyscrasias, immunodeficiency, and diabetes, among others) that will contraindicate the surgical procedure
* patients taking medications known to interfere with the wound healing process or that contraindicate the surgical procedure
* smokers or pregnant women
* patients who underwent periodontal surgery in the area of interest.
What they're measuring
1
Percentage of Defect Coverage
Timeframe: 6 months
Trial details
NCT IDNCT02817763
SponsorUniversidade Estadual Paulista Júlio de Mesquita Filho