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Conservative Versus Conventional Restorative Approach for Endodontically Treated Posterior Teeth

2 ottobre 2026 aggiornato da: 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.

Panoramica dello studio

Descrizione dettagliata

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 di studio

Interventistico

Iscrizione (Stimato)

50

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Luoghi di studio

    • Manial
      • Cairo, Manial, Egitto

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

Da 20 anni a 50 anni (Adulto)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

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

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Separare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Comparatore attivo: 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.

Altro: 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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
clinical evaluation of tooth integrity
Lasso di tempo: 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

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Patient satisfaction
Lasso di tempo: 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

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Pubblicazioni generali

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

20 settembre 2025

Completamento primario (Stimato)

1 giugno 2027

Completamento dello studio (Stimato)

1 giugno 2027

Date di iscrizione allo studio

Primo inviato

14 settembre 2026

Primo inviato che soddisfa i criteri di controllo qualità

17 settembre 2026

Primo Inserito (Effettivo)

23 settembre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

6 ottobre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

2 ottobre 2026

Ultimo verificato

1 settembre 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

INDECISO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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