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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05777811
Other study ID # Buccal Vestibule Depth
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 3, 2021
Est. completion date January 15, 2023

Study information

Verified date March 2023
Source Hacettepe University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this comparative trial, 50 patients with shallow vestibules and Type 1/2 recessions will be treated with either a vertically coronally advanced flap + connective tissue graft or a free gingival graft. At baseline, 3rd-month, 6th-month, and 12th-month visits, the following parameters will be evaluated: buccal vestibular depth, keratinized tissue height, gingival thickness, recession depth, recession width, probing depth, and clinical attachment level. Keratinized tissue change, gingival thickness change, root coverage, clinical attachment gain, and complete root coverage will be calculated. The wound healing index, tissue appearance, patient expectations, aesthetics, and dentin hypersensitivity will be assessed at baseline and at the 6th week.


Description:

Buccal vestibule depth was recorded using two different measurement methods. First, the distance between the cementoenamel junction and the deepest point of the vestibule sulcus was measured and recorded as VD1. Then, the distance between the gingival margin and the base of the vestibule sulcus was measured and recorded as VD2.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date January 15, 2023
Est. primary completion date January 3, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - full-mouth plaque and bleeding scores <15% - the presence of at least one recession type-1/2 recession and at least one recession with recession depth = 2 mm - the presence of an identifiable cemento-enamel junction Exclusion Criteria: - Vestibule depth > 6mm - Smoking > 10 cigarettes per day - Any contraindications for periodontal surgery - Unstable endodontic conditions or presence of any restoration.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Vertically coronally advanced flap combined with connective tissue graft.
The exposed root surfaces are planed with Gracey 1-2 curettes. An intrasulcular incision is made with a blade on the buccal aspects of the involved teeth. The incision is extended horizontally to the adjacent papilla. Then, slightly divergent vertical releasing incisions are carried 2 mm beyond the mucogingival junction. A full-thickness flap is raised with a periosteal elevator towards the mucogingival junction. After that, a partial-thickness dissection is carried out in the apical direction to release muscle tension and provide coronal advancement of the flap. The adjacent papillae are de-epithelialized. The connective tissue graft (CTG) is harvested from the lateral palate using the de-epithelialized gingival graft technique. After harvesting, the connective tissue graft is sutured to the recipient bed. Finally, the flap is positioned 2 mm over the cementoenamel junction and sutured with 6-0 polypropylene sutures. No periodontal dressing is applied.
Free gingival graft
A partial-thickness flap is elevated (using a blade #15c) with horizontal incisions at the cemento-enamel junction (CEJ) level of the adjacent teeth. Then, two vertical incisions extending to the apical are made from the two ends of the horizontal incision. The epithelium in the framed region is removed with a scalpel, and the underlying connective tissue is exposed. To achieve the best vascularization of the free gingival graft from the recipient site, bed preparation is completed with a split-thickness horizontal incision that joins the vertical incisions in the apical region. The free gingival graft is stabilized using interrupted sutures and a sling suture.

Locations

Country Name City State
Turkey Hacettepe University Ankara

Sponsors (1)

Lead Sponsor Collaborator
Hacettepe University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Vestibule depth 2 The distance between the free gingival margin and the most apical point of the vestibul. Baseline
Primary Vestibule depth 2 The distance between the free gingival margin and the most apical point of the vestibul. 3rd month
Primary Vestibule depth 2 The distance between the free gingival margin and the most apical point of the vestibul. 6th month
Primary Vestibule depth 2 The distance between the free gingival margin and the most apical point of the vestibul. 12th month.
Primary Vestibule depth 1 The distance between the free semento-enamel junction and the most apical point of the vestibul. Baseline
Primary Vestibule depth 1 The distance between the free semento enamel junction and the most apical point of the vestibul. 3rd month
Primary Vestibule depth 1 The distance between the free semento-enamel junction and the most apical point of the vestibul. 6th month
Primary Vestibule depth 1 The distance between the free semento-enamel junction and the most apical point of the vestibul. 12th month
Secondary Recession depth (RD) Measured as the distance from the cementoenamel junction to the gingival margin Baseline
Secondary Recession depth (RD) Measured as the distance from the cementoenamel junction to the gingival margin 6th week
Secondary Recession depth (RD) Measured as the distance from the cementoenamel junction to the gingival margin 6th month.
Secondary Recession depth (RD) Measured as the distance from the cementoenamel junction to the gingival margin 12th month.
Secondary Probing depth (PD) Measures as the distance from the apical of gingival sulcus to the gingival margin. Baseline
Secondary Probing depth (PD) Measures as the distance from the apical of gingival sulcus to the gingival margin. 6th week
Secondary Probing depth (PD) Measures as the distance from the apical of gingival sulcus to the gingival margin. 6th month
Secondary Probing depth (PD) Measures as the distance from the apical of gingival sulcus to the gingival margin. 12th month.
Secondary Clinical attachment level (CAL) measured as the distance from th tip of the probe inserted into the sulcus to de cementoenamel junction. Baseline.
Secondary Clinical attachment level (CAL) measured as the distance from th tip of the probe inserted into the sulcus to de cementoenamel junction. 6th week
Secondary Clinical attachment level (CAL) measured as the distance from th tip of the probe inserted into the sulcus to de cementoenamel junction. 6th month
Secondary Clinical attachment level (CAL) measured as the distance from th tip of the probe inserted into the sulcus to de cementoenamel junction. 12th month.
Secondary Keratinized tissue height (KTH) measured from the most apical point of the recession at the gingival margin to the mucogingival line. Baseline.
Secondary Keratinized tissue height (KTH) measured from the most apical point of the recession at the gingival margin to the mucogingival line. 6th week
Secondary Keratinized tissue height (KTH) measured from the most apical point of the recession at the gingival margin to the mucogingival line. 6th month
Secondary Keratinized tissue height (KTH) measured from the most apical point of the recession at the gingival margin to the mucogingival line. 12th month.
Secondary Gingival thickness (GT) determined 1.5 mm apical to the gingival margin, measured with the caliper accurete to the nearest 0.1 mm. Baseline.
Secondary Gingival thickness (GT) determined 1.5 mm apical to the gingival margin, measured with the caliper accurete to the nearest 0.1 mm. 6th week.
Secondary Gingival thickness (GT) determined 1.5 mm apical to the gingival margin, measured with the caliper accurete to the nearest 0.1 mm. 6th month.
Secondary Gingival thickness (GT) determined 1.5 mm apical to the gingival margin, measured with the caliper accurete to the nearest 0.1 mm. 12th month.
Secondary Wound healing index (WHI) Wound healing index (WHI) was recorded two-weeks after surgery. The wound surface was visually inspected and the soft tissue healing was defined as 'uneventful' (score 1), 'slightly disturbed' (score 2) or 'poor' (score 3) based on the presence and severity of the items including patient discomfort, erythema, edema, suppuration and flap dehiscence. 2nd week
Secondary Tissue appearance (TA) Tissue appearance (TA) was evaluated by asking the patients to score the consistency, contour, color match, keloid formation degree and contiguity of their treated sites at T2. The scores were collected as points, shown in parentheses, by asking the consistency as firm (1p) or spongy (0p); contour as presence (2p) or absence (0p) of knife-edged and scalloped gingival margin; color match as excellent (3p), good (2p), adequate (1p) or unsatisfactory (0p); keloid formation degree as absent (1p) or present (0p); contiguity as the presence (-1p) or absence (0p) of each perceptible incision mark. 6th week
Secondary Dentine hypersensitivity (DH) Dentine hypersensitivity (DH) was evaluated with air evaporative stimulus method at baseline and T2. After placement of finger(s) for preserving the nearby teeth, the recession sites were subjected to evaporative stimulus comprised of 1-second air blast from 1 to 3 mm distance by using the air spray at 40-65 psi pressure and 19±50C. After application, the patients were requested to give a score to their DH between 0 (=no pain) and 10 (=extreme pain). 6th week
Secondary Patient expectations (PE) Patient expectations (PE) were evaluated by requesting from the patients to rate their treatment results at T2, as satisfactory or not, in terms of appearance, experience and obtained root coverage. 6th week
Secondary Aesthetics (A) Aesthetics (A) was evaluated by the patient at T1 by rating its level as excellent, good, fair or poor. 6th week
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