Questa pagina è stata tradotta automaticamente e l'accuratezza della traduzione non è garantita. Si prega di fare riferimento al Versione inglese per un testo di partenza.

Clinical Performance and Fit of 3D-Printed Versus Milled Endocrowns: An 18-Month Trial (Endocrowns)

12 luglio 2026 aggiornato da: Yara Ahmed Elgammal, October 6 University

Clinical Performance and Restoration Fit of 3D-Printed Versus Milled Biomimetic Resin Composite Endocrowns: 18-Month Randomized Clinical Trial.

The goal of this clinical trial is to learn whether 3D-printed resin composite endocrowns perform as well as milled resin composite endocrowns in restoring endodontically treated teeth. It will also learn how well the restorations fit over time.

The main questions it aims to answer are:

Do 3D-printed endocrowns and milled endocrowns show different clinical performance? Do 3D-printed endocrowns and milled endocrowns differ in restoration fit over 18 months?

Researchers will compare two fabrication methods:

Additive manufacturing: 3D-printed resin composite endocrowns. Subtractive manufacturing: milled resin composite endocrowns.

Participants will:

Be recruited from the Conservative Dentistry Department, Faculty of Dentistry, October 6 University.

Receive tooth preparation after confirmation of satisfactory root canal treatment.

Have their teeth prepared using standardized endocrown guidelines by one calibrated operator.

Have digital scans taken of the prepared tooth, opposing arch, and bite registration.

Have restorations designed digitally and then assigned randomly to one of the two groups.

Receive a temporary restoration until the final endocrown is ready.

Have the final restoration tried in for fit, contacts, and occlusion before cementation.

Have a baseline post-cementation scan taken for fit assessment.

Return for follow-up visits at baseline, 6 months, 12 months, and 18 months.

Be evaluated at each visit using Modified FDI criteria and 3D digital superimposition for fit analysis.

Panoramica dello studio

Descrizione dettagliata

Eligible participants will be recruited from the Conservative Dentistry Department, Faculty of Dentistry, October 6 University.

Following confirmation of satisfactory root canal treatment. Tooth preparation will follow standardized endocrown guidelines. All preparations will be performed by a single calibrated operator (Y.A.E.).

Full-arch digital impressions will be captured using an intraoral scanner, including scans of the prepared tooth, opposing arch, and bite registration. Digital files (STL format) will be used to design definitive restorations in CAD software. Following digital design, participants will be randomly allocated (1:1 ratio) to one of two fabrication groups:

Group 1 (Intervention): Additive manufacturing (3D-printed resin composite) Group 2 (Comparator): Subtractive manufacturing (milled resin composite) Teeth will be temporized with intermediate restorative material, then temporary materials will be removed and preparations cleaned. Restorations will be tried to verify fit, contacts, and occlusion.

After cementation, scan the seated restoration with the same intraoral scanner to create baseline restoration STL file (T0) for longitudinal fit assessment. Participants will be recalled at baseline (T0), 6 months (T1), 12 months (T2) and18 months (T3). At each visit, restorations will be evaluated using Modified FDI criteria (clinical performance) and 3D digital superimposition (Restoration fit via Geomagic Control X)

Tipo di studio

Interventistico

Iscrizione (Stimato)

52

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

Luoghi di studio

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

  • Adulto

Accetta volontari sani

Descrizione

Inclusion Criteria:

- Patient-Related Criteria

  1. Age: Between 20 and 40 years.
  2. Oral Hygiene: Good oral hygiene, evidenced by low plaque and gingival index scores.
  3. Willingness to attend regular follow-up visits during the study period

    - Tooth-Related Criteria

  4. Endodontic Quality: High-quality root canal treatment with no clinical or radiographic signs of pathology.
  5. Tooth Type: A permanent molar tooth requiring an endocrown after successful root canal treatment.
  6. Located in functional occlusion and opposing natural teeth in stable occlusal contact with the restored tooth.
  7. Teeth free from cracks, fractures, or internal resorption; supporting tissues without structural defects that may compromise restoration success

Exclusion Criteria:

- Patient-Related Criteria

  1. Parafunctional Habits: Severe bruxism, clenching, or other parafunctional habits.
  2. Allergies: to any study materials (e.g., resin composites, bonding agents).
  3. Patients with systemic diseases contraindicate elective dental treatment (e.g., uncontrolled diabetes)

    - Tooth-Related Criteria

  4. Insufficient Tooth Structure: Less than 2mm of circumferential sound denting height or deep, unrestorable.
  5. Tooth opposes prosthetic restoration.
  6. Teeth with a history of fixed prosthetic restorations (previous crowns, inlays/onlays, or bridge restorations)
  7. Periodontal Issues: Active periodontal disease, excessive mobility (> Grade 1, or a hopeless long-term prognosis.

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: Doppio

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Altro: Milled resin composite restorations fabricated using subtractive manufacturing from CAD/CAM blocks.
Subtractive Manufacturing, the control group will utilize restorations fabricated via subtractive manufacturing, specifically by milling from industrially fabricated blocks of nanohybrid composite. This method is the established gold standard for producing CAD/CAM resin composite restorations. It is known for creating restorations with excellent mechanical properties, high density, and predictable clinical performance due to the optimized, industrial-grade polymerization of the blocks. These materials, which include polymer-infiltrated ceramic networks (PICNs) and resin nanoceramics, were developed to combine the favorable properties of both ceramics and resin composites, offering a biomimetic alternative to traditional glass-ceramics.
Subtractive Manufacturing, the control group will utilize restorations fabricated via subtractive manufacturing, specifically by milling from industrially fabricated blocks of nanohybrid composite. This method is the established gold standard for producing CAD/CAM resin composite restorations. It is known for creating restorations with excellent mechanical properties, high density, and predictable clinical performance due to the optimized, industrial-grade polymerization of the blocks. These materials, which include polymer-infiltrated ceramic networks (PICNs) and resin nanoceramics, were developed to combine the favorable properties of both ceramics and resin composites, offering a biomimetic alternative to traditional glass-ceramics.
Additive Manufacturing, the intervention group will feature restorations fabricated via 3D printing. This technology is more time and cost-efficient, more accurate, and could provide a considerable alternative to the currently applied CNC milling, reduced material waste, and the ability to create complex geometries with high precision. Recent studies have shown that 3D-printed restorations can achieve promising results in terms of marginal and internal fit, which are critical for clinical longevity. This has spurred the development of novel, ceramic-filled hybrid materials specifically engineered for permanent 3D-printed restorations. Manufacturers of these materials claim high dimensional stability, flexural strength, and a modulus suitable for definitive restorations (e.g., Bego; VarseoSmile Triniq technical product data sheet). However, there is a lack of clinical data to support these claims.
Altro: Three dimensionally (3D) printed resin composite restorations fabricated using additive manufacturi
Additive Manufacturing, the intervention group will feature restorations fabricated via 3D printing. This technology is more time and cost-efficient, more accurate, and could provide a considerable alternative to the currently applied CNC milling, reduced material waste, and the ability to create complex geometries with high precision. Recent studies have shown that 3D-printed restorations can achieve promising results in terms of marginal and internal fit, which are critical for clinical longevity. This has spurred the development of novel, ceramic-filled hybrid materials specifically engineered for permanent 3D-printed restorations. Manufacturers of these materials claim high dimensional stability, flexural strength, and a modulus suitable for definitive restorations (e.g., Bego; VarseoSmile Triniq technical product data sheet). However, there is a lack of clinical data to support these claims.
Subtractive Manufacturing, the control group will utilize restorations fabricated via subtractive manufacturing, specifically by milling from industrially fabricated blocks of nanohybrid composite. This method is the established gold standard for producing CAD/CAM resin composite restorations. It is known for creating restorations with excellent mechanical properties, high density, and predictable clinical performance due to the optimized, industrial-grade polymerization of the blocks. These materials, which include polymer-infiltrated ceramic networks (PICNs) and resin nanoceramics, were developed to combine the favorable properties of both ceramics and resin composites, offering a biomimetic alternative to traditional glass-ceramics.
Additive Manufacturing, the intervention group will feature restorations fabricated via 3D printing. This technology is more time and cost-efficient, more accurate, and could provide a considerable alternative to the currently applied CNC milling, reduced material waste, and the ability to create complex geometries with high precision. Recent studies have shown that 3D-printed restorations can achieve promising results in terms of marginal and internal fit, which are critical for clinical longevity. This has spurred the development of novel, ceramic-filled hybrid materials specifically engineered for permanent 3D-printed restorations. Manufacturers of these materials claim high dimensional stability, flexural strength, and a modulus suitable for definitive restorations (e.g., Bego; VarseoSmile Triniq technical product data sheet). However, there is a lack of clinical data to support these claims.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Clinical performance
Lasso di tempo: T0=baseline (1st week), T1=6 months, T2=12 months and T3=18 months follow-up.

World Dental Federation (FDI) criteria set to evaluate direct and indirect dental restorations: Hickel et al. (2023).

Aesthetic properties of Endocrown restorations (Domain A):

  1. Surface Luster
  2. Staining (surface, margin)
  3. color match and translucency
  4. Esthetic anatomical form

    Functional performance of Endocrown restorations (Domain F):

  5. Fracture of material and retention
  6. Marginal adaptation
  7. Approximal anatomical form

    Biological Properties of Endocrown restorations (Domain B):

  8. Recurrence of caries (CAR)
  9. Tooth integrity (enamel cracks, tooth fracture)
  10. Periodontal response
T0=baseline (1st week), T1=6 months, T2=12 months and T3=18 months follow-up.

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Restoration Fit
Lasso di tempo: T0=baseline (1st week), T1=6 months, T2=12 months and T3=18 months follow-up.
  1. Marginal Adaptation
  2. Internal Adaptation Triple-scan digital superimposition (Geomagic Control X 2022 software)
T0=baseline (1st week), T1=6 months, T2=12 months and T3=18 months follow-up.

Collaboratori e investigatori

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

Investigatori

  • Direttore dello studio: Mohsen Hussein Abielhassan, • Professor, Conservative Dent, October 6 University

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

  • 7. Cal, I. K., Ozturk, F., Aydin, N., & Karaoglanoglu, S. (2024). 3D Printed Restorations Produced From Permanent Resin: Case Report. International Dental Journal, 74, S298. 10.1016/j.identj.2024.07.282 8. Doumit, M., Beuer, F., Böse, M. W. H., Unkovskiy, A., Hey, J., & Prause, E. (2025). Wear behavior of 3D printed, minimally invasive restorations: Clinical data after 24 months in function. The Journal of Prosthetic Dentistry, 134(3), 662-669. 10.1016/j.prosdent.2025.03.014 9. Güntekin, N., & Tunçdemir, A. R. (2024). Comparison of volumetric loss and surface roughness of composite dental restorations obtained by additive and subtractive manufacturing methods. Heliyon, 10(4). 10.1016/j.heliyon.2024.e26269 10. Hickel, R., Mesinger, S., Opdam, N., Loomans, B., Frankenberger, R., Cadenaro, M., . & Kühnisch, J. (2023). Revised FDI criteria for evaluating direct and indirect dental restorations-recommendations for its clinical use, interpretation, and reporting. Clinical oral investigations, 27(6), 2573-2592. 10.1007/s00784-022- 04814-1 11. Kader, İ. T., Özer, S., & Arıcan, B. (2025). The effect of different fit-indicating materials and preparation designs on the marginal and internal fit of 3D-printed permanent endocrowns. Meandros Medical And Dental Journal, 26(1), 108-116. 10.69601/meandrosmdj.1596545 12. Koyuturk, A. E., Ozmen, B., Tokay, U., Tuloglu, N., Sari, M. E., & Sonmez, T. T. (2013). Two-year follow-up of indirect posterior composite restorations of permanent teeth with excessive material loss in pediatric patients: a clinical study. Journal of Adhesive Dentistry, 15(6). 10.3290/j.jad.a30897 13. Mahran, G. A., El-Banna, A., & El-Korashy, D. I. (2025). Evaluation of a 3Dprinted nanohybrid resin composite versus a milled resin composite for flexural strength, wear and color stability. BMC Oral Health, 25(1), 572. https://doi.org/10.1186/s12903-025-05861-2
  • 1.Abad-Coronel, C., Durán Urdiales, D., Benalcázar Arias, M. V., Córdova, A. K., Medina, M. S., & Bravo Torres, W. (2025). Flexural strength, fatigue behavior, and microhardness of three-dimensional (3D)-printed resin material for indirect restorations: A systematic review. Materials, 18(3), 556. https://doi.org/10.3390/ma18030556 2. Abou-steit, S. S., Salem, M. A., Omar, S., & Mahmoud, N. (2024). Clinical evaluation of the biomimetic aspect in the restoration of endodontically treated teeth (Randomized clinical trial). Egyptian Dental Journal, 70(3), 2683-2693. 10.21608/EDJ.2024.291267.3045 3. Abuabboud, O., Marinescu, A. G., Paven, M., Kovacs, I. M., Nica, L. M., Faur, A. B., & Jivănescu, A. (2025). Influence of Cement Thickness, Dentine Thickness, and Intracoronal Depth on the Fracture Resistance of 3D-Printed Endocrowns: A Pilot In Vitro Study. Dentistry Journal, 13(6), 263. 10.3390/dj13060263 23 4. Albrecht, M., Schmidt, F., Menzel, F., Yassine, J., Beuer, F., & Unkovskiy, A. (2024). Comparative Analysis of Modern 3D-Printed Hybrid Resin-Ceramic Materials for Indirect Restorations: An In Vitro Study. Polymers,16(22), 3161. https://doi.org/10.3390/polym16223161 5. Alghauli, M. A., & Alqutaibi, A. Y. (2024). 3D-printed intracoronal restorations, occlusal and laminate veneers: Clinical relevance, properties, and behavior compared to milled restorations; a systematic review and meta-analysis. Journal of Esthetic and Restorative Dentistry, 36(8), 1153-1170. 10.1111/jerd.13228 6. Arslan, S., Karagön, M., Balkaya, H., & Köse, B. (2024). A randomized clinical study evaluating the 30-month clinical performance of class II indirect restorations in endodontically treated teeth using ceramic, hybrid, and composite computer-aided design/computer-aided production blocks. Journal of Conservative Dentistry and Endodontics, 27(1), 68-75. 10.4103/JCDE.JCDE_213_23

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 (Stimato)

1 novembre 2026

Completamento primario (Stimato)

1 novembre 2028

Completamento dello studio (Stimato)

1 dicembre 2028

Date di iscrizione allo studio

Primo inviato

12 luglio 2026

Primo inviato che soddisfa i criteri di controllo qualità

12 luglio 2026

Primo Inserito (Effettivo)

16 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

16 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

12 luglio 2026

Ultimo verificato

1 luglio 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 .

3
Sottoscrivi