N/A
N=40
A New Surgical-restorative Approach to Treat Gingival Recessions Associated With Non-carious Cervical Lesions (NCCL)
Gingival Recession · Tooth Abrasion
Bottom Line
View on ClinicalTrials.gov: NCT02817763 ↗Enrolled (actual)
40
Serious AEs
0.0%
Results posted
Jun 2017
Primary outcome: Primary: Percentage of Defect Coverage — 15; 14 Gingival recessions
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Connective tissue graft (CTG) (Procedure); CTG plus resin composite restoration (Procedure); sodium dipyrone (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Universidade Estadual Paulista Júlio de Mesquita Filho
- Primary completion
- Oct 2015
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Percentage of Defect Coverage |
15; 14 | — |
| SECONDARY Modified Root Coverage Esthetic Score (MRES) |
7.13; 8.71 | — |
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.
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.