Gingival Recession Clinical Trial
Official title:
Evaluation of Two Different Flaps Associated With Connective Tissue Graft in the Treatment of Gingival Recession: A Randomized Clinical Trial
The aim of this study was to compare clinical, esthetic and patient-centered outcomes of coronally advanced tunnel (TUN) and coronally advanced flap (CAF) both associated with connective tissue graft (CTG) in the treatment of gingival recession.
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.
Patients were assigned to one of the three treatment groups:
- Group TUN+CTG (21): Periodontal surgery for root coverage through tunnel flap technique
plus connective tissue graft.
- Group CAF+CTG (21): Periodontal surgery for root coverage through trapezoidal flap plus
connective tissue graft.
All surgical procedures were performed by a single operator (MPS). The gingival recession
defects were randomly treated by either the trapezoidal-type of coronally advanced flap plus
connective tissue graft (CAF+CTG) or the coronally advanced tunnel technique with
subepithelial connective tissue graft (TUN+CTG). In brief description, CAF treatment was
performed by starting with two divergent releasing incisions lateral to the recessed area. A
sulcular incision was made to unite the releasing incisions and the flap was raised beyond
the mucogingival junction (MGJ) in split-full-split thickness. The connective tissue graft
was removed from the palate and sutured in position. Sling sutures were placed to stabilize
the flap in a coronal position 2 mm above the cement-enamel junction (CEJ), followed by
interrupted sutures to close the releasing incisions. The tunnel flap was performed with
initial sulcular incisions, spit thickness flap was prepared using specific tunneling knives
beyond the mucogingival junction and until flap gain mobility. The flap was laterally
extended to adjacent papillae that were carefully detached by means of a full-thickness
preparation. The connective tissue graft was insert into the tunnel. Sling sutures were
performed involving the flap and graft to coronally cover 2 mm above the CEJ. After the
surgery, the participants were requested to take 500 mg of sodium dipyrone every 4 hours for
3 days in case of pain, and to avoid brushing and flossing in the treated area for a period
of 2 weeks. During this period, plaque control was performed using 0.12% chlorhexidine rinse
used twice a day. The sutures were removed after 7 days, and all of the patients were
recalled for prophylaxis and reinforcement of motivation and instruction for atraumatic tooth
brushing during the study period.
Clinical, esthetics, and comfort of patients parameters were assessed at 45 days, 2, 3 and 6
months after the procedure.
Quantitative data were recorded as mean ± standard deviation (SD), and normality was tested
using Shapiro-Wilk tests. The probing depth (PD), relative gingival recession (RGR), clinical
attachment level (CAL), keratinized tissue thickness (KTT), keratinized tissue width (KTW),
and dentin hypersensitivity (DH) values were examined by two-way repeated measures ANOVA to
evaluate the differences within and between groups, followed by a Tukey test for multiple
comparisons when the Shapiro-Wilk p value was ≥ 0.05. 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 visual
analog scale (VAS) were analyzed by T-tests. The frequency of complete root coverage was
compared using χ2 tests. Intergroup root coverage esthetic score (RES) comparisons were
performed with a T-test. A significance level of 0.05 was adopted.
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