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Intraoral Aging of 3D Printed Orthodontic Aligners

5 novembre 2026 mis à jour par: Azza Gamal Kamel Wafa, Alexandria University

The Effect of Intraoral Aging on 3D-Printed Aligners: A Randomized Split-Mouth Study

This study aims to bridge the gap in literature by conducting a combined evaluation of the mechanical, chemical, optical, and morphological changes of 3D-printed clear aligners manufactured from TC-85 and TA-28 resins that occur after clinical use. By analyzing aligners retrieved after two weeks of intraoral use, this research will offer critical insights into the material stability and aging behavior of the two types of 3D-printed clear aligners.

Aperçu de l'étude

Description détaillée

Background: Direct 3D-printing of clear aligners is emerging as a promising alternative to conventional thermoformed systems, offering enhanced precision, digital workflow efficiency, and improved material control. Among the photopolymer resins used for 3D-printed aligners, Tera Harz TC-85 and Tera Harz TA-28 have emerged as leading materials due to their reported shape-memory behavior, dimensional stability, and mechanical performance. However, despite increasing clinical adoption, limited evidence exists regarding how these two materials respond to intraoral aging, where fluctuating pH, temperature changes, salivary enzymes, and occlusal forces may alter their mechanical, optical, chemical, and surface characteristics. Understanding these changes is essential for determining the clinical reliability and long-term performance of each resin.Therefore, a demanding evaluation of post-aging changes in 3D-printed aligners is essential to determine their suitability for sustained orthodontic force delivery and to guide material selection in clinical practice. Assessing how key properties such as mechanical behavior, dimensional accuracy, surface topography, and optical characteristics evolve after intraoral exposure will provide valuable insight into material durability and clinical reliability.

Type d'étude

Interventionnel

Inscription (Réel)

12

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

    • Alexandria Governorate
      • Alexandria, Alexandria Governorate, Egypte, 21526
        • Department of Orthodontics, Faculty of Dentistry, Alexandria University

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans à 35 ans (Adulte)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  • Patients aged 18-35 years.
  • Mild to moderate crowding.
  • Good oral hygiene and healthy periodontium.
  • Permanent dentition with no active caries.

Exclusion Criteria:

  • Patients with systemic diseases affecting saliva or oral mucosa.
  • Smoking or alcohol consumption.
  • History of parafunctional habits.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Science basique
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation croisée
  • Masquage: Double

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: TC-85 maxillary / TA-28 mandibular

Participants received a directly 3D-printed TC-85 aligner in the maxillary arch and a directly 3D-printed TA-28 aligner in the mandibular arch. Both aligners were worn simultaneously for 2 weeks (22 hours/day).

Aligner directly 3D-printed from Tera Harz TC-85 shape-memory resin [add printer, layer thickness and post-curing protocol]. Worn 22 hours/day for 2 weeks in the maxillary or mandibular arch, according to a computer-generated randomization sequence.

Expérimental: TA-28 maxillary / TC-85 mandibular

Participants received a directly 3D-printed TA-28 aligner in the maxillary arch and a directly 3D-printed TC-85 aligner in the mandibular arch. Both aligners were worn simultaneously for 2 weeks (22 hours/day).

Aligner directly 3D-printed from Tera Harz TA-28 shape-memory resin [same printer, layer thickness and post-curing protocol as above]. Worn 22 hours/day for 2 weeks in the maxillary or mandibular arch, according to a computer-generated randomization sequence.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Change in indentation hardness (HIT), measured by instrumented nanoindentation
Délai: Baseline (unused aligner) and after 2 weeks of intraoral use

Indentation hardness (HIT, GPa) of directly 3D-printed TC-85 and TA-28 aligners, measured by instrumented nanoindentation using a Nano Indenter XP (MTS Systems Corporation, USA) with a Berkovich diamond indenter. Tests were displacement-controlled to a maximum depth of 2000 nm at a constant strain rate of 0.05 s-¹, with 25 indentations per specimen spaced 30 μm apart. Testing followed ISO 14577-1:2015 and data were analyzed by the Oliver and Pharr method. Retrieved aligners are compared with unused aligners printed from the same digital design.

Baseline (unused aligner) and after 2 weeks of intraoral use

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Change in indentation elastic modulus (EIT), measured by instrumented nanoindentation
Délai: Baseline (unused aligner) and after 2 weeks of intraoral use

Indentation elastic modulus (EIT, GPa) of directly 3D-printed TC-85 and TA-28 aligners, measured by instrumented nanoindentation using a Nano Indenter XP (MTS Systems Corporation, USA) with a Berkovich diamond indenter. Tests were displacement-controlled to a maximum depth of 2000 nm at a constant strain rate of 0.05 s-¹, with 25 indentations per specimen spaced 30 μm apart. A Poisson's ratio of 0.4 was assumed. Testing followed ISO 14577-1:2015 and data were analyzed by the Oliver and Pharr method. Retrieved aligners are compared with unused aligners printed from the same digital design.

Baseline (unused aligner) and after 2 weeks of intraoral use
Change in color (ΔE₀₀, CIEDE2000), measured by UV-visible spectrophotometry
Délai: Baseline (unused aligner) and after 2 weeks of intraoral use

Color of directly 3D-printed TC-85 and TA-28 aligners measured with a UV-visible spectrophotometer (V-770, JASCO Corporation, Tokyo, Japan). Each aligner was sectioned along the right central incisor-canine region, and the labial surface was positioned in a standardized manner facing the incident-light window. CIE Lab* coordinates were recorded according to ISO 11664-4:2019, and the color change between unused and retrieved aligners was calculated as ΔE₀₀ using the CIEDE2000 equation (parametric factors set to 1). Values are interpreted against 0.8 (50:50% perceptibility) and 1.8 (50:50% acceptability).

Baseline (unused aligner) and after 2 weeks of intraoral use
Change in light transmittance and absorbance (400-700 nm), measured by UV-visible spectrophotometry
Délai: Baseline (unused aligner) and after 2 weeks of intraoral use

Light transmittance and absorbance of TC-85 and TA-28 aligners recorded across the visible range (400-700 nm) with a UV-visible spectrophotometer (V-770, JASCO Corporation, Tokyo, Japan) using Spectra Manager II software, after calibration according to the manufacturer's instructions. Values at 400 and 700 nm were extracted from each spectrum and compared between materials and between unused and retrieved aligners.

Baseline (unused aligner) and after 2 weeks of intraoral use
Change in aligner thickness (μm), measured by confocal laser scanning microscopy
Délai: Baseline (unused aligner) and after 2 weeks of intraoral use

Thickness of TC-85 and TA-28 aligners measured by confocal laser scanning microscopy (Leica DMi8, Leica Microsystems, Wetzlar, Germany) with a 10× objective and 1.5× digital zoom under standardized imaging conditions. Standardized 4 × 4 mm specimens were taken from the labial surface of the left central incisor region. Z-stack images were reconstructed in 3D using Leica LAS AF software (version 1.1.0.12420), and thickness was calculated as the perpendicular distance between the upper and lower specimen surfaces. Each specimen was measured twice and the mean was used.

Baseline (unused aligner) and after 2 weeks of intraoral use
Change in surface roughness (Sa, Sq, Sp, Sv), measured by confocal laser scanning microscopy
Délai: Baseline (unused aligner) and after 2 weeks of intraoral use

Surface roughness of the inner surface of directly 3D-printed TC-85 and TA-28 aligners, assessed on the same 4 × 4 mm specimens used for thickness measurement, imaged by confocal laser scanning microscopy (Leica DMi8, Leica Microsystems, Wetzlar, Germany). Height maps generated from the z-stacks with Leica LAS AF software were analyzed in ImageJ (National Institutes of Health, USA) with the SurfCharJ-1q plugin to calculate Sa (arithmetical mean height), Sq (root mean square height), Sp (maximum peak height) and Sv (maximum valley depth), in µm. Analysis was repeated twice per specimen and the mean was used. Identical acquisition and analysis settings were applied to all specimens.

Baseline (unused aligner) and after 2 weeks of intraoral use
Change in degree of conversion (DC), measured by ATR-FTIR spectroscopy
Délai: Baseline (unused aligner) and after 2 weeks of intraoral use

Degree of conversion (%) of TC-85 and TA-28 aligners, calculated from attenuated total reflectance Fourier-transform infrared (ATR-FTIR) spectra as the reduction of the aliphatic C=C band near 1638 cm-¹ relative to, referenced to the corresponding unset resin. Retrieved aligners are compared with unused aligners.

Baseline (unused aligner) and after 2 weeks of intraoral use
Change in chemical structure, assessed by ATR-FTIR spectral analysis
Délai: Baseline (unused aligner) and after 2 weeks of intraoral use

Qualitative comparison of ATR-FTIR spectra of unused and retrieved TC-85 and TA-28 aligners, focusing on the O-H/N-H stretching bands (3400-3200 cm-¹), aliphatic C-H bands (about 2920 and 2850 cm-¹), the carbonyl (C=O) band (about 1700 cm-¹) and the C-O/C-O-C region (1200-1000 cm-¹).

Baseline (unused aligner) and after 2 weeks of intraoral use

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

  • Chercheur principal: Azza Gamal Wafa, PHD, Alexandria University

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

1 février 2026

Achèvement primaire (Réel)

1 avril 2026

Achèvement de l'étude (Réel)

1 septembre 2026

Dates d'inscription aux études

Première soumission

31 octobre 2026

Première soumission répondant aux critères de contrôle qualité

5 novembre 2026

Première publication (Réel)

9 novembre 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

9 novembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

5 novembre 2026

Dernière vérification

1 janvier 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

INDÉCIS

Description du régime IPD

Individual participant data will not be shared publicly because of participant confidentiality and privacy considerations. The study involves a relatively small sample, and sharing individual-level data may pose a risk of participant identification. De-identified aggregate results will be reported in the published manuscripts. Data may be made available from the corresponding author upon reasonable request, subject to institutional ethical approval and applicable data-protection requirements.

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

produit fabriqué et exporté des États-Unis.

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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