Volume-Stable Collagen Matrix Versus Subepithelial Connective Tissue Graft for Multiple Gingival Recessions (VCMX-SCTG)
Volume-Stable Xenogeneic Collagen Matrix Versus Subepithelial Connective Tissue Graft for the Treatment of Multiple Gingival Recessions: A 12-Month Randomized Controlled Clinical Trial
Gingival recession is a clinical condition in which the gingival margin is displaced apically, exposing the root surface. This condition may be associated with esthetic concerns, dentin hypersensitivity, and difficulties in oral hygiene. Subepithelial connective tissue grafting is considered a standard surgical approach for root coverage, but it requires harvesting tissue from the palate, which may increase postoperative discomfort. Volume-stable xenogeneic collagen matrices have been proposed as an alternative biomaterial to reduce the need for a palatal donor site.
This randomized controlled clinical trial will compare a volume-stable xenogeneic collagen matrix with an autogenous subepithelial connective tissue graft for the treatment of multiple gingival recessions. Participants will be allocated to one of two treatment groups. The test group will receive root coverage surgery using a volume-stable collagen matrix, while the control group will receive root coverage surgery using a subepithelial connective tissue graft. Clinical, patient-reported, esthetic, and digital outcomes will be assessed at baseline and during follow-up visits up to 12 months.
The primary outcome will be the change in gingival recession depth from baseline to 12 months. Secondary outcomes will include keratinized tissue width, gingival thickness, percentage of root coverage, complete root coverage, dentin hypersensitivity, patient-reported satisfaction, early wound healing, and digital volumetric changes assessed by intraoral scanning.
Aperçu de l'étude
Statut
Les conditions
Description détaillée
This study is a randomized controlled clinical trial designed to evaluate the clinical performance of a volume-stable xenogeneic collagen matrix compared with an autogenous subepithelial connective tissue graft in the treatment of multiple gingival recessions.
Eligible participants presenting multiple gingival recessions will be recruited and allocated to one of two parallel treatment groups. In the test group, participants will receive root coverage surgery using a volume-stable xenogeneic collagen matrix associated with a coronally advanced flap. In the control group, participants will receive root coverage surgery using an autogenous subepithelial connective tissue graft associated with a coronally advanced flap.
Clinical assessments will include gingival recession depth, keratinized tissue width, probing depth, clinical attachment level, gingival thickness, percentage of root coverage, and complete root coverage. Patient-reported outcomes will include dentin hypersensitivity, postoperative comfort, esthetic satisfaction, and acceptance of the procedure. Standardized clinical photographs and intraoral scans will be obtained during follow-up. Digital analyses will be used to assess changes in soft tissue volume over time.
The primary endpoint will be the change in gingival recession depth from baseline to 12 months. Secondary endpoints will include clinical, esthetic, patient-reported, wound healing, and digital volumetric outcomes assessed at predefined follow-up visits.
Type d'étude
Inscription (Estimé)
Phase
- N'est pas applicable
Contacts et emplacements
Coordonnées de l'étude
- Nom: Edgar Daniel Vargas Quiroga, DDS, MSc
- Numéro de téléphone: +551633153000
- E-mail: edgar.vargasquiroga@usp.br
Sauvegarde des contacts de l'étude
- Nom: Arthur Belem Novaes Jr, DDS, PhD
- E-mail: novaesjr@forp.usp.br
Lieux d'étude
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São Paulo
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Ribeirão Preto, São Paulo, Brésil, 14040-904
- School of Dentistry of Ribeirão Preto, University of Sao Paulo
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Contact:
- Edgar Daniel Vargas Quiroga, DDS, MSc
- Numéro de téléphone: +551633153000
- E-mail: edgar.vargasquiroga@usp.br
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Contact:
- Arthur Belem Novaes Jr, DDS, PhD
- E-mail: novaesjr@forp.usp.br
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Chercheur principal:
- Arthur Belem Novaes Jr, DDS, PhD
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Sous-enquêteur:
- Edgar Daniel Vargas Quiroga, DDS, MSc
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
La description
Inclusion Criteria:
- Adults aged 18 years or older.
- Presence of at least two Cairo RT1 gingival recessions in anterior teeth and/or premolars.
- Gingival recession depth greater than or equal to 2 mm.
- Presence of at least 2 mm of keratinized gingiva apical to the gingival recession.
- Indication for root coverage treatment due to esthetic concern and/or dentin hypersensitivity.
- Sites with non-carious cervical lesions may be included if they are previously restored and, after restoration, present residual gingival recession greater than or equal to 2 mm.
- Good plaque control, defined as full-mouth plaque score and full-mouth marginal gingival bleeding score below 20%.
Exclusion Criteria:
- Current smokers or individuals who stopped smoking less than 12 months before enrollment.
- Decompensated systemic diseases.
- Pregnancy or lactation.
- Active periodontal disease.
- Untreated root caries.
- Previous mucogingival surgery in the study area.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Seul
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Expérimental: Volume-Stable Collagen Matrix
Participants in this group will receive root coverage surgery using a volume-stable xenogeneic collagen matrix associated with a coronally advanced flap.
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A volume-stable xenogeneic collagen matrix will be used as a soft-tissue substitute for root coverage surgery.
The matrix will be placed over the recession defects and covered by a coronally advanced flap.
Autres noms:
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Comparateur actif: Subepithelial Connective Tissue Graft
Participants in this group will receive root coverage surgery using an autogenous subepithelial connective tissue graft associated with a coronally advanced flap.
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An autogenous subepithelial connective tissue graft will be harvested from the palate and used for root coverage surgery.
The graft will be placed over the recession defects and covered by a coronally advanced flap.
Autres noms:
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Gingival Recession Depth
Délai: Baseline, 3 months, 6 months, and 12 months
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Gingival recession depth will be measured clinically in millimeters as the distance from the cementoenamel junction to the gingival margin.
The main comparison between groups will be performed at 12 months.
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Baseline, 3 months, 6 months, and 12 months
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Gingival Recession Width
Délai: Baseline, 3 months, 6 months, and 12 months
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Gingival recession width will be measured horizontally in millimeters at the level of the cementoenamel junction.
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Baseline, 3 months, 6 months, and 12 months
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Keratinized Tissue Width
Délai: Baseline, 3 months, 6 months, and 12 months
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Keratinized tissue width will be measured in millimeters from the gingival margin to the mucogingival junction.
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Baseline, 3 months, 6 months, and 12 months
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Gingival Thickness
Délai: Baseline, 3 months, 6 months, and 12 months
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Gingival thickness will be measured in millimeters at the treated sites using a standardized clinical method.
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Baseline, 3 months, 6 months, and 12 months
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Probing Depth
Délai: Baseline, 3 months, 6 months, and 12 months
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Probing depth will be measured in millimeters from the gingival margin to the bottom of the sulcus or pocket at the treated sites.
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Baseline, 3 months, 6 months, and 12 months
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Clinical Attachment Level
Délai: Baseline, 3 months, 6 months, and 12 months
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Clinical attachment level will be calculated in millimeters as probing depth plus gingival recession depth.
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Baseline, 3 months, 6 months, and 12 months
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Percentage of Root Coverage
Délai: 3 months, 6 months, and 12 months
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Percentage of root coverage will be calculated based on the reduction in gingival recession depth from baseline to 12 months.
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3 months, 6 months, and 12 months
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Complete Root Coverage
Délai: 3 months, 6 months, and 12 months
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Complete root coverage will be defined as the absence of residual gingival recession at the treated site.
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3 months, 6 months, and 12 months
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Dentin Hypersensitivity
Délai: Baseline, 3 months, 6 months, and 12 months
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Will be assessed after standardized air stimulation using a 0 to 100 visual analog scale.
A score of 0 indicates no pain or sensitivity, and a score of 100 indicates the worst imaginable pain or sensitivity.
Higher scores indicate worse dentin hypersensitivity.
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Baseline, 3 months, 6 months, and 12 months
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Patient-Reported Esthetic Satisfaction
Délai: Baseline, 3 months, 6 months, and 12 months
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Patient-reported esthetic satisfaction will be assessed using a 0 to 100 visual analog scale.
A score of 0 indicates complete dissatisfaction, and a score of 100 indicates complete satisfaction.
Higher scores indicate better esthetic satisfaction.
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Baseline, 3 months, 6 months, and 12 months
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Digital Volumetric Changes
Délai: Baseline, 3 months, 6 months, and 12 months
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Soft tissue volumetric changes will be assessed using intraoral scans and digital superimposition of three-dimensional Standard Tessellation Language (STL) models.
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Baseline, 3 months, 6 months, and 12 months
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Early Wound Healing
Délai: 7 days, 14 days, and 30 days
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Early wound healing will be assessed clinically during the postoperative period based on flap margin adaptation, suture stability, edema, inflammation, erythema, fibrin accumulation, tissue necrosis, epithelialization, biomaterial or graft exposure, and overall wound healing pattern.
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7 days, 14 days, and 30 days
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Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Arthur Belem Novaes Jr, DDS, PhD, University of Sao Paulo
- Chaise d'étude: Edgar Daniel Vargas Quiroga, DDS, MSc, University of Sao Paulo
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- CAAE 98199226.9.0000.5419 (Autre identifiant: Plataforma Brasil / Brazilian CEP-CONEP System)
Plan pour les données individuelles des participants (IPD)
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Description du régime IPD
Informations sur les médicaments et les dispositifs, documents d'étude
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