Gingival Recession Clinical Trial
Official title:
Evaluation of a New Surgical-restorative Approach for the Treatment of Gingival Recessions Associated With Non-carious Cervical Lesions: a Randomized Controlled Clinical Trial
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.
This was a prospective, parallel and controlled clinical trial.
- Group CTG (control n = 20) - patients who received connective tissue graft to treat
gingival recession associated with non-carious cervical lesion. Group CTG+RC (test n = 20) -
patients who received connective tissue graft plus partial resin composite restoration to
treat gingival recession associated with non-carious cervical lesion.
The surgeries, as well as all postoperative follow-up, were performed at the dental clinic of
Institute of Science and Technology (ICT), State University of São Paulo (UNESP). For those
recessions allocated to CTG group, 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 CTG group. Afterwards, a thin and small connective tissue graft was removed
from the palatal site and sutured over the root surface. Then, the flap was coronally
positioned and sutured to completely cover the graft. For those recessions allocated to
CTG+RC group, firstly a sterile rubber dam was placed to isolate the operative field and the
coronal zone of the non-carious cervical lesion restoration was performed with a
nanocomposite resin, following the manufacturer's instructions. The apical margin of the
restoration was place 1 millimeter apically to the cemento-enamel junction estimation. In the
following session the CTG+RC received the surgical procedure as described above where a thin
and small connective tissue graft was removed from the palatal site and 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.
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