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Conservative Versus Conventional Restorative Approach for Endodontically Treated Posterior Teeth

2 de outubro de 2026 atualizado por: Moataz Mostafa Anwar

Clinical Evaluation of the Conservative Versus Conventional Restorative Approach for Endodontically Treated Posterior Teeth: A Randomized Clinical Trial

This study compares two methods of restoring posterior teeth after root canal treatment. Traditionally, dentists use fiber posts and full coverage crowns, but this requires removing more tooth structure, which can weaken teeth further. A newer, more conservative option is the overlay, which preserves more of the natural tooth. While overlays appear promising, evidence is still limited, particularly for posterior teeth.

The trial, conducted at Cairo University, will involve fifty patients aged 20-50 with properly root canal treated posterior teeth. Participants will be randomly divided into two groups: one receiving a fiber-reinforced composite with a lithium disilicate overlay (conservative method), and the other receiving a fiber post, composite core, and full coverage lithium disilicate crown (conventional method).

The primary outcome will be tooth integrity after six months, evaluated with standardized criteria. Secondary outcomes include margin quality, discoloration, secondary decay, color matching, and patient satisfaction. Patients will be blinded to the treatment they receive, and data will be analyzed using appropriate statistical methods.

Visão geral do estudo

Descrição detalhada

This research protocol explores two different ways of restoring posterior teeth after root canal treatment. Teeth that have had root canal treatment often become weaker because part of their natural structure is removed, and the dentin itself becomes more fragile. As a result, these teeth are more likely to break. Dentists have usually treated this problem by placing a fiber post inside the root canal and then covering the tooth with a full coverage crown. This method has worked well, but it involves drilling inside the root canal, which can make the tooth weaker on the long run.

With advances in modern dentistry, new techniques aim to be more conservative; they try to save as much of the natural tooth as possible. One of these approaches is the overlay, a type of partial coverage restoration that seats on top of the tooth but does not require as much removal of healthy structure as a full coverage crown. Recent studies suggest that overlays can perform just as well as crowns, but there is still not enough strong clinical evidence to confirm this for all cases, especially for posterior teeth that face heavy biting forces. This trial will help fill that gap in the literature.

The study will take place at the Faculty of Dentistry, Cairo University, and will include fifty patients aged between 20 and 50 years. All patients must have had root canal treatment on a restorable posterior tooth. Those with poorly treated canals, cracked teeth, gum disease, or bruxism will not be included. Patients who join the trial will be divided randomly into two groups. One group will receive the conservative approach: the cavity will be filled with fiber-reinforced composite, and the tooth will be prepared for a lithium disilicate overlay. The other group will follow the conventional method: a fiber post will be placed, a composite build-up added, and finally the tooth will be covered with a full coverage lithium disilicate crown.

The main goal is to see how well each method keeps the tooth intact after six months, using a standard set of criteria to judge success. Other factors will also be checked, such as how well the margins fit, whether there is discoloration or secondary decay, and whether the color matches the surrounding teeth. Importantly, patients will also be asked how satisfied they are with the treatment, using a simple scale to record their feelings.

To make sure the study is fair, patients will be randomly assigned to one of the two groups using a computer program. The operator performing the treatment will know which method is being used, but the patients and the statistician analyzing the results will not, which helps reduce bias. Data will be collected carefully and stored securely. Standard statistical methods will be used to analyze the results, with differences considered significant if the probability of chance is 5% or less.

All patients will sign a consent before joining. Any possible side effects, such as minor discomfort, will be noted. After the six-month follow-up, results will be published in scientific journals and conferences.

By comparing these two approaches, the study hopes to show whether the conservative overlay technique can be a reliable alternative to the traditional crown. If proven successful, this method could help dentists save more of the natural tooth structure, reduce treatment time, and still provide durable, esthetic, and satisfying results for patients.

Tipo de estudo

Intervencional

Inscrição (Estimado)

50

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.

Contato de estudo

Estude backup de contato

Locais de estudo

    • Manial
      • Cairo, Manial, Egito
        • Recrutamento
        • Faculty of Dentistry, Cairo University
        • Contato:

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

20 anos a 50 anos (Adulto)

Aceita Voluntários Saudáveis

Não

Gêneros Elegíveis para o Estudo

Tudo

Descrição

Inclusion Criteria:

  1. Patients 20-50 years of age
  2. Root canal treated posterior teeth
  3. Good C/R ratio
  4. Good quality root canal treatment (adequate working length, absence of post operative complications or pain and adequate follow up period)
  5. Presence of adequate labial and palatal wall thickness
  6. Natural antagonist teeth
  7. Natural adjacent teeth

Exclusion Criteria:

  1. Improper root canal treatment
  2. Post operative complications.
  3. Cracked teeth
  4. Parafunctional habits (bruxism)
  5. Wear pattern
  6. Pregnancy for females
  7. Opposing prosthetics
  8. Presence of periodontal disease
  9. Severely destructed posterior teeth

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: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Solteiro

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Comparador Ativo: Fiber reinforced composite core and lithium disilicate overlay

This arm implements a restorative approach that combines the mechanical support of a fiber-reinforced composite (FRC) core with the esthetic and durable properties of a lithium disilicate overlay. The FRC core provides internal reinforcement, distributing stresses within the tooth and enhancing fracture resistance, while the lithium disilicate overlay offers high strength, wear resistance, and excellent optical qualities.

This intervention implements a restorative approach that combines the mechanical support of a fiber-reinforced composite (FRC) core with the esthetic and durable properties of a lithium disilicate overlay. The FRC core provides internal reinforcement, distributing stresses within the tooth and enhancing fracture resistance, while the lithium disilicate overlay offers high strength, wear resistance, and excellent optical qualities.

Outro: Fiber post with composite core build up and lithium disilicate full coverage crown

This arm combines the intraradicular retention of a fiber post with a composite core build-up, providing internal support and reinforcement for compromised teeth. The restoration is completed with a lithium disilicate full coverage crown, offering high strength, durability, and excellent esthetics.

This combines the intraradicular retention of a fiber post with a composite core build-up, providing internal support and reinforcement for compromised teeth. The restoration is completed with a lithium disilicate full coverage crown, offering high strength, durability, and excellent esthetics.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
clinical evaluation of tooth integrity
Prazo: 6 months

Clinical evaluation of tooth integrity will be measured according to the modified USPHS Criteria having scores of either Alpha, Bravo or Charlie. This will be repeated during the time frame of the Study.

6 months

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Patient satisfaction
Prazo: 6 months

This outcome will be measured through handing the participants a questionnaire addressing the function, color and overall quality and acceptance of the final restorations.

6 months

Colaboradores e Investigadores

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

Patrocinador

Publicações e links úteis

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Publicações Gerais

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)

20 de setembro de 2025

Conclusão Primária (Estimado)

1 de junho de 2027

Conclusão do estudo (Estimado)

1 de junho de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

14 de setembro de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

17 de setembro de 2026

Primeira postagem (Real)

23 de setembro de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

6 de outubro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

2 de outubro de 2026

Última verificação

1 de setembro de 2026

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

INDECISO

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

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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