The trial will be performed as a prospective, randomized and controlled, single-blind
investigation to study clinical parameters and patients' experiences when performing a
frenectomy, comparing diode laser treatment with the conventional scalpel technique.
Participants:
This study will include 43 participants who will be identified with aberrant papillary
frenum attachment according to Mirko et al., and will be referred to the periodontology
department. The inclusion criteria for the participants will be:
All participants will sign a written informed consent form before participating in the
study.
Study Groups and Randomization:
Before any surgical procedure, all subjects will undergo a thorough medical and dental
history review, as well as intraoral and radiographic examinations. Participants who
match the inclusion criteria will be provided with oral hygiene instructions tailored to
their specific needs. Initially, the clinical periodontal parameters of all participants
will be measured. Then, a mechanical cleaning procedure will be carried out using an
ultrasonic scaler (CavitronÒ; Dentsply International) and hand instruments (Gracey, 5/6,
7/8, 11/12, 13/14; Hu-Friedy Ins. Co.). A total of 43 participants will be enrolled in
the study and assigned to one of two groups using a computer-based randomization table
(www.graphpad.com/quickcalcs). The participants will be randomly divided into two groups:
the experimental group, which will undergo diode laser surgery (L=20), and the control
group, which will undergo conventional scalpel surgery (C=23).
Post-treatment Procedure:
After the frenectomy procedures in all groups, patients will receive oral hygiene
instructions and will be advised to consume soft and cold food for the next 12 hours.
Additionally, a 0.12% chlorhexidine gluconate mouth rinse will be prescribed to be used
once a day for one minute over five days. For pain relief, 500 mg of acetaminophen (1-2
tablets) will be prescribed as needed, with patients instructed to record the dosage and
frequency of use.
Clinical Evaluation:
Z.T.E. will perform all surgical procedures, while a calibrated single examiner (K.Y)
will perform all clinical evaluations. Patients in the C group will undergo primary wound
healing with sutures, whereas patients in the L group will not get any sutures.
Therefore, neither the clinicians (Z.T.E and K.Y) nor the patients will be kept unaware
of the study's details over the entire duration. In order to ensure consistency in the
measurements of K.Y, a calibration exercise was conducted until the agreement coefficient
achieves a level of 90%. This calibration process was consist of evaluating three
patients on two separate occasions within a 24-hour period. The calibration was
considered effective if the variation between repeated measurements of periodontal
keratinized gingival width (KGW) at the beginning and after 24 hours is less than 3%. The
clinical periodontal parameters, such as the plaque index (PI), gingival index (GI), and
periodontal pocket depth (PD), will be measured using a periodontal probe from the
University of North Carolina (PCPUNC15; Hu-Friedy Ins. Co.). At baseline and at
postoperative week 6 and month 6, all periodontal measurements will be taken at six sites
per tooth as part of a full-mouth evaluation. KGW on teeth 11 and 12, the heights of the
interdental papillae between the incisors (from the tip of an interdental papilla to the
line joining the lowest points on the gingival margins of adjacent incisors), interdental
papilla width, and the amount of diastema will be measured at baseline and at month 6.
Before the operations, the labial frenulum attachments will be classified into four
types: I - mucosal attachment; II - gingival attachment; III - papillary attachment; and
IV - papilla penetrating attachment. Pain will be evaluated using the visual analogue
scale (VAS) on postoperative days 1, 3, 7, 14, 21, and 28. The scale will be comprised of
a horizontal line with values ranging from '0' to '10', where '0' indicates the absence
of pain and '10' indicates the presence of severe discomfort.
Statistical Analysis:
Each patient will be accepted as one statistical unit and the statistical analysis will
be performed by SPSS 20 (SPSS Corporation, Chicago, IL) with a significance level p <
0.05. The Kolmogorov-Smirnov test will be used to check the distribution for normality.
Repeated measurements of clinical parameters will be analyzed with Friedman test and
Wilcoxon signed-rank test. The Kruskal-Wallis, Chi-square, and Fisher's exact tests will
be used to determine differences among the groups. Moreover, in case of significant
difference among groups, the Mann-Whitney U test will be used to compare two groups by
Bonferroni correction.