Gingival Recession Clinical Trial
Official title:
Comparison of Different Surgical Approaches for Root Coverage of Teeth Presenting With Gingival Recession Associated With Non-carious Cervical Lesion Partially Restored With Composite Resin. Randomized Controlled Clinical Trial
The aim of the present study is to compare the use of the xenogeneic graft (MC) plus coronary advanced flap (CAF) and the coronary advanced flap alone, both associated with the partial restoration of composite resin in the treatment of gingival recessions associated with non-carious cervical lesion.
This is a prospective, parallel and controlled clinical trial. The population evaluated in
the study was selected at Institute of Science and Technology (ICT), São José dos Campos,
College of Dentistry.
Sixty patients presenting gingival recession will be divided in 2 groups:
- Group 1 - Test: 30 gingival recessions associated with non-carious cervical lesions that
will receive partial composite resin restoration and periodontal surgery for root
coverage through a xenogenic collagen matrix graft (CAF + MC + R)
- Group 2 - control: 30 gingival recessions associated with non-carious cervical lesions
that will receive partial composite resin restoration and periodontal surgery for root
coverage (CAF + R) without graft.
The surgeries, as well as all postoperative follow-up, were performed at the dental clinic of
ICT. Two horizontal incisions were made at right angles to the adjacent interdental papillae,
without interfering with the gingival margins of neighboring teeth. Two oblique vertical
incisions were extended beyond the mucogingival junction, and a trapezoidal mucoperiosteal
flap was raised up to the mucogingival junction. After this point, a split-thickness flap was
extended apically, releasing the tension and favoring coronal positioning of the flap.The
exposed root surface was gently scaled and planed until it became smooth in the connective
tissue graft (CTG) group. For those allocated to CTG plus composite resin (CR) group, a
sterile rubber dam was placed to isolate the operative field and the non-carious cervical
lesion restoration was performed with a nanocomposite resin (Filtek Supreme - 3M - St. Paul,
Minnesota, USA), following the manufacturer's instructions. Afterward, the both groups
received a thin and small connective tissue graft that was sutured over the root/restoration
surface. Then, the flap was coronally positioned and sutured to completely cover the graft.
Clinical parameters were assessed at baseline and 3 and 6 months post-operatively.
Statistical Analysis The null hypothesis considered in the study was the absence of
difference in the clinical parameters between the different groups. For data analysis, the
statistical program was used (SigmaPlot). The demographic and clinical data were compared
between the groups using Student's t-test. The data were first analyzed for homogeneity using
the Shapiro-Wilk test, which indicated non-normal distribution. . Those presenting
Shapiro-Wilk p values < 0.05 were analyzed using a Friedman test (for intragroup comparisons)
and Mann-Whitney tests (for intergroup comparisons). Patients' esthetics and discomfort
measures using a visual analog scale (VAS) were analyzed by T-tests. The frequency of sites
that were scored as very good or excellent in each group by qualitative cosmetic evaluation
(QCE) analysis, the frequency of complete root coverage, bleeding on probing (BOP), and the
presence or absence of plaque at the site were compared using χ2 tests. Intergroup root
esthetic scale (RES) comparisons were performed with a T-test. A significance level of 0.05
was adopted.
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