N/A
Completed N=40
A New Surgical-restorative Approach to Treat Gingival Recessions Associated With Non-carious Cervical Lesions (NCCL)
Gingival Recession · Tooth Abrasion
Source: ClinicalTrials.gov NCT02817763 ↗
Enrolled (actual)
40
Serious AEs
0.0%
Results posted
Jun 2017
Primary outcomePrimary: Percentage of Defect Coverage — 15; 14 Gingival recessions
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.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Percentage of Defect Coverage |
15; 14 | — |
| SECONDARY Modified Root Coverage Esthetic Score (MRES) |
7.13; 8.71 | — |
Eligibility Criteria
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 ˂ 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.
Data sourced from ClinicalTrials.gov (NCT02817763). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.