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Deep Margin Elevation in Endodontically Treated Posterior Teeth (DME-PERIO)

30 de junho de 2026 atualizado por: Büşra Kara Yıldız, Hacettepe University

Evaluation of Periodontal Response on Proximal Surfaces With Deep Margin Elevation in CAD/CAM Restorations of Endodontically Treated Posterior Teeth

This study aims to evaluate the periodontal response of proximal surfaces with deep margin elevation (DME) in endodontically treated posterior teeth restored with CAD/CAM systems. Deep subgingival margins present clinical challenges in terms of isolation, restoration, and long-term periodontal health.

DME is a minimally invasive technique used to relocate subgingival margins coronally to a supragingival level, facilitating adhesive procedures and CAD/CAM restoration placement. However, the periodontal effects of DME remain unclear.

In this prospective split-tooth clinical study, proximal surfaces treated with DME will be compared with control surfaces without DME within the same tooth. The primary outcome will be bleeding on probing (BOP), while secondary outcomes will include probing depth and plaque index. Clinical and radiographic evaluations will be performed at baseline and during follow-up.

The results of this study are expected to provide clinical evidence regarding the periodontal impact of DME and support clinical decision-making in the restoration of endodontically treated posterior teeth.

Visão geral do estudo

Descrição detalhada

This prospective split-tooth controlled clinical study aims to evaluate the periodontal response associated with deep margin elevation (DME) in endodontically treated posterior teeth restored with CAD/CAM systems.

Endodontically treated teeth frequently present with extensive structural loss due to caries, previous restorations, or endodontic access cavity preparation, which compromises the structural integrity of the tooth. In such cases, deep subgingival margins are commonly encountered, making isolation, adhesive procedures, and restorative treatment more challenging. Deep margin elevation (DME) is a minimally invasive technique used to relocate subgingival margins coronally to the cemento-enamel junction level using resin composite, facilitating adhesive procedures, digital impression taking, and CAD/CAM restoration placement. However, the periodontal effects of DME remain unclear and require further clinical investigation.

A total of 45 restorations will be included in patients aged between 18 and 65 years who present with at least one endodontically treated posterior tooth with extensive coronal destruction. A split-tooth design will be used, where one proximal surface requiring deep margin elevation will be assigned as the test surface (DME), while the opposing proximal surface with supragingival or equigingival margin will serve as the control.

All clinical procedures will be performed at the Department of Restorative Dentistry, Faculty of Dentistry, Hacettepe University. Before treatment, professional cleaning will be performed using a pumice-water mixture and polishing instruments to remove plaque accumulation. All restorative procedures will be carried out under rubber dam isolation using ×3 magnification dental loupes.

During the DME procedure, isolation will be achieved using a sectional matrix system and wedges. A universal adhesive system (G-Premio Bond, GC, Tokyo, Japan) will be applied following enamel conditioning with 37% phosphoric acid for 10-15 seconds. The subgingival margin will then be elevated to the enamel level using a high-filled injectable composite resin (G-ænial Universal Injectable, GC, Tokyo, Japan).

All restorations will be fabricated using a chairside CAD/CAM system (CEREC Omnicam, Dentsply Sirona, Bensheim, Germany) and milled from a resin nanoceramic hybrid block (Cerasmart 270, GC, Tokyo, Japan) according to the manufacturer's instructions.

The internal surface of the restoration will be sandblasted with 50 µm aluminum oxide, cleaned with alcohol, and treated with G-CEM ONE Adhesive Primer (GC, Tokyo, Japan). The tooth surface will be conditioned with 37% phosphoric acid, followed by the application of G-Premio Bond. Restorations will be luted using a self-adhesive resin cement (G-CEM ONE, GC, Tokyo, Japan). Excess cement will be removed after short light exposure, and final polymerization will be performed using a high-intensity LED curing unit (Bluephase N, Ivoclar Vivadent), with 10 seconds of curing per surface.

Finishing and polishing procedures will be completed using fine diamond burs, aluminum oxide-coated polishing discs, and polishing systems. Occlusion will be checked and adjusted when necessary.

Periodontal parameters will be recorded at baseline (T0) and at follow-up visits at 1 week, 6 months, and 12 months. The primary outcome measure will be bleeding on probing (BOP), assessed at six sites per tooth, and the presence of bleeding at any site will be recorded as positive. Secondary outcome measures will include probing pocket depth (PPD) measured in millimeters and plaque index (PI). Gingival index (GI) will also be recorded as an additional parameter.

Restorations will be evaluated according to FDI criteria by two calibrated clinicians who are blinded to the intervention. Functional, biological, esthetic, and patient-related parameters will be assessed. Patient satisfaction will be evaluated using a 5-point Likert scale including general, esthetic, and functional satisfaction.

Sample size calculation was performed using G*Power 3.1 software based on McNemar test assumptions for paired data (α=0.05, power=80%). Based on estimated discordant proportions (p10=0.27 and p01=0.03), the minimum required sample size was calculated as 40 teeth. Considering a potential 10% dropout rate, a total of 45 restorations will be included.

Statistical analysis will be performed using SPSS software. Differences in BOP between test and control surfaces will be analyzed using the McNemar test. PPD and PI values will be analyzed using the Wilcoxon signed-rank test. Changes over time will also be evaluated using paired statistical methods. A significance level of p<0.05 will be considered statistically significant.

This study is expected to provide clinically relevant evidence regarding the periodontal effects of deep margin elevation and contribute to evidence-based decision-making in the restorative management of endodontically treated posterior teeth.

Tipo de estudo

Intervencional

Inscrição (Estimado)

45

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

      • Ankara, Turquia (Türkiye)
        • Hacettepe University, Faculty of Dentistry, Department of Restorative Dentistry

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Descrição

Inclusion Criteria:

  • Patients aged between 18 and 65 years
  • Presence of at least one endodontically treated posterior tooth (premolar or molar) with extensive coronal structure loss
  • Teeth indicated for indirect CAD/CAM restoration
  • Presence of at least one proximal surface requiring deep margin elevation (subgingival margin)
  • Opposing proximal surface with supragingival or equigingival margin suitable as control
  • Good general health and ability to attend follow-up visits
  • Signed informed consent

Exclusion Criteria:

  • Patients with poor oral hygiene or uncontrolled periodontal disease
  • Presence of active periodontal disease requiring treatment
  • Teeth with mobility greater than Grade I
  • Teeth with periapical pathology or unsuccessful endodontic treatment
  • Patients with systemic diseases affecting periodontal health (e.g., uncontrolled diabetes)
  • Pregnant or lactating women
  • Patients using medications affecting gingival tissues (e.g., immunosuppressants, calcium channel blockers)
  • Heavy smokers
  • Patients unable to comply with follow-up schedule

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Não randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Deep Margin Elevation
Proximal surfaces treated with deep margin elevation (DME) using a resin composite to relocate subgingival margins to a supragingival level prior to CAD/CAM restoration.
Deep margin elevation (DME) is performed by relocating subgingival proximal margins coronally using a high-filled injectable composite resin following adhesive procedures, prior to CAD/CAM restoration placement.
Comparador Ativo: Control (No DME)
Proximal surfaces restored without deep margin elevation, where margins are located at supragingival or equigingival levels.
Restorative treatment is performed without deep margin elevation, where proximal margins remain at supragingival or equigingival levels and are restored using CAD/CAM systems.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Bleeding on Probing (BOP) Positive Surface Proportion
Prazo: Baseline (1 week post-treatment), 6 months, and 12 months
Gingival inflammation will be assessed by measuring Bleeding on Probing (BOP) using a periodontal probe at six sites per tooth (mesio-buccal, mesio-lingual, mid-buccal, mid-lingual, disto-buccal, and disto-lingual) . The presence of bleeding at any site within the proximal area will be recorded as positive . The proportion of BOP-positive surfaces will be compared between the deep margin elevation (DME) surfaces (experimental group) and the non-DME supragingival surfaces (control group) on the same tooth.
Baseline (1 week post-treatment), 6 months, and 12 months

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Changes in Periodontal Pocket Depth (PPD)
Prazo: Baseline (1 week post-treatment), 6 months, and 12 months
Periodontal pocket depth (PPD) will be measured in millimeters using a periodontal probe at the same six sites per tooth (mesio-buccal, mesio-lingual, mid-buccal, mid-lingual, disto-buccal, and disto-lingual) . The distance from the gingival margin to the bottom of the periodontal pocket will be recorded to evaluate dimensional changes over time and compare DME vs. control surfaces.
Baseline (1 week post-treatment), 6 months, and 12 months
Plaque Index (PI) Scores
Prazo: Baseline (1 week post-treatment), 6 months, and 12 months

Gingival plaque accumulation will be evaluated at the evaluated proximal surfaces using the Silness and Löe Plaque Index scoring system.This ordinal index scores plaque retention specifically at the marginal area to assess oral hygiene correlation with the restorations.

Plaque Index (PI) Scores: Plaque Index is assessed using the Silness and Löe Plaque Index, with scores ranging from 0 to 3, where 0 = no plaque, 1 = a film of plaque adhering to the free gingival margin and adjacent tooth surface, 2 = moderate accumulation of plaque, and 3 = abundant plaque accumulation. Higher scores indicate worse oral hygiene.

Baseline (1 week post-treatment), 6 months, and 12 months
Gingival Index (GI) Scores
Prazo: Baseline (1 week post-treatment), 6 months, and 12 months

Clinical evaluation of gingival health will be performed using the Löe and Silness Gingival Index[cite: 1]. The assessment will be conducted at both the deep margin elevation (DME) surface and the non-DME proximal surface using a periodontal probe to grade tissue condition and inflammation severity.

Gingival Index (GI) Scores: Gingival health is assessed using the Löe and Silness Gingival Index, with scores ranging from 0 to 3, where 0 = normal gingiva, 1 = mild inflammation, 2 = moderate inflammation with bleeding on probing, and 3 = severe inflammation with spontaneous bleeding. Higher scores indicate worse gingival health.

Baseline (1 week post-treatment), 6 months, and 12 months
Clinical Performance of CAD/CAM Endocrowns using FDI Criteria
Prazo: 1 week (Baseline), 6 months, and 12 months post-treatment

The clinical quality and success of the Cerasmart 270 hybrid ceramic endocrown restorations will be evaluated by two calibrated independent examiners using the World Dental Federation (FDI) criteria[cite: 1]. The assessment covers functional criteria (retention, fracture, marginal adaptation, proximal contact), biological criteria (secondary caries, tooth integrity), and aesthetic criteria (color match, surface gloss) using a 5-point scoring system.

Clinical Performance of CAD/CAM Endocrowns using FDI Criteria: Clinical performance is assessed using the FDI World Dental Federation Clinical Criteria for the Evaluation of Direct and Indirect Restorations. Each criterion is scored on a 5-point scale (1-5), where 1 = clinically excellent/very good, 2 = clinically good, 3 = clinically satisfactory, 4 = clinically unsatisfactory but repairable, and 5 = clinically poor (replacement required). Higher scores indicate worse clinical performance of the restoration.

1 week (Baseline), 6 months, and 12 months post-treatment

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Patrocinador

Investigadores

  • Diretor de estudo: Şükran Bolay, Prof., Hacettepe University
  • Investigador principal: Büşra Kara Yıldız, Hacettepe University

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

24 de março de 2026

Conclusão Primária (Estimado)

24 de outubro de 2026

Conclusão do estudo (Estimado)

24 de abril de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

20 de abril de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

16 de junho de 2026

Primeira postagem (Real)

22 de junho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

2 de julho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

30 de junho de 2026

Última verificação

1 de junho de 2026

Mais Informações

Termos relacionados a este estudo

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

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