Esta página foi traduzida automaticamente e a precisão da tradução não é garantida. Por favor, consulte o versão em inglês para um texto fonte.

Comparison of Single-Layer and Triple-Layer TPU MaxFlex Aligners After Intraoral Use (TPU-ALIGN)

27 de abril de 2026 atualizado por: Abdul Qadir, Ayub Medical College, Abbottabad

Effects of Intraoral Aging on Mechanical Properties and Surface Morphology of Single-Layer Versus Triple-Layer Thermoplastic Polyurethane (TPU) MaxFlex Aligner Sheets: A Randomized Controlled Trial

This study aims to compare two types of clear orthodontic aligner materials used in dental treatment: single-layer and triple-layer thermoplastic polyurethane (TPU) aligners (MaxFlex). Clear aligners are commonly used to straighten teeth and are preferred for their comfort and aesthetic appearance.

Participants will be provided with aligners and instructed to wear them for approximately 22 hours per day for 10 days. The aligners will be collected before use and after the 10-day period. The study will evaluate how the oral environment affects the properties of these materials over time.

Laboratory tests will be conducted to measure mechanical properties such as strength, flexibility, and deformation, as well as to examine surface changes under a microscope. The results of this study may help improve the performance and durability of aligners and contribute to better orthodontic treatment outcomes.

Visão geral do estudo

Descrição detalhada

Clear aligner therapy (CAT) has become an increasingly popular alternative to fixed orthodontic appliances due to its aesthetic advantages, improved patient comfort, and ease of oral hygiene maintenance. Thermoplastic materials, particularly thermoplastic polyurethane (TPU), are widely used in the fabrication of aligners due to their favorable mechanical and elastic properties.

Recent advancements in aligner materials have led to the development of multilayer TPU systems designed to enhance flexibility, force delivery, and clinical performance. Triple-layer TPU aligners typically consist of a soft inner layer for patient comfort, a rigid intermediate layer for structural strength, and a flexible outer layer to improve adaptability and fit. In contrast, single-layer TPU aligners are composed of a homogeneous material and are generally more cost-effective.

Despite these developments, limited evidence exists regarding the comparative behavior of single-layer and multilayer TPU materials following intraoral exposure. The oral environment, characterized by temperature fluctuations, moisture, masticatory forces, and enzymatic activity, may contribute to material degradation, potentially affecting aligner performance.

This randomized controlled trial is designed to evaluate the effects of intraoral aging on the mechanical properties and surface morphology of single-layer and triple-layer TPU aligners (MaxFlex). Participants will be randomly assigned to receive one type of aligner material and will be instructed to wear the aligners for a standardized duration of 10 days (minimum 22 hours per day).

Aligners will be collected at baseline (prior to intraoral use) and after the 10-day wear period. Following retrieval, samples will undergo standardized cleaning procedures before laboratory analysis.

Mechanical testing will be performed using dynamic mechanical analysis to assess tensile properties, stress relaxation behavior, and creep characteristics. Surface morphology will be evaluated using scanning electron microscopy to identify features such as roughness, cracks, and voids. Additionally, Fourier transform infrared spectroscopy will be used to detect potential chemical changes in the material composition.

The primary objective of this study is to compare the mechanical performance of single-layer and triple-layer TPU aligners before and after intraoral use. Secondary outcomes include evaluation of surface morphology and chemical structure changes associated with intraoral aging.

The findings of this study are expected to provide insight into the durability and clinical performance of different aligner materials, which may help guide material selection and improve orthodontic treatment outcomes.

Tipo de estudo

Intervencional

Inscrição (Real)

66

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

    • Punjab Province
      • Lahore, Punjab Province, Paquistão
        • Akhtar Saeed Medical & Dental College

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

Aceita Voluntários Saudáveis

Não

Descrição

Inclusion Criteria:

Patients aged 18-30 years Fully erupted permanent dentition Good periodontal health Patients undergoing orthodontic treatment with clear aligners Mild crowding or spacing requiring labiolingual tooth movement Willingness to wear aligners for at least 22 hours per day Provision of informed consent

Exclusion Criteria:

Use of aligners from manufacturers other than study-specific TPU aligners Damaged or fractured aligners Poor compliance (wear time less than 22 hours/day) Presence of parafunctional habits (e.g., bruxism) Hypodontia or partially erupted dentition Cases involving bonded attachments on maxillary incisors Cases requiring rotational movement of maxillary incisors Patients with systemic or oral conditions affecting saliva composition or the oral environment

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

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Single-Layer TPU Aligner Group
Participants in this group will receive single-layer thermoplastic polyurethane (TPU) MaxFlex aligners. The aligners will be worn intraorally for 10 days for a minimum of 22 hours per day under standardized conditions. Aligners will be collected at baseline and after the wear period for evaluation of mechanical properties and surface morphology.
Single-layer thermoplastic polyurethane (TPU) clear aligners fabricated from a homogeneous TPU sheet using thermoforming techniques. These aligners are designed to deliver orthodontic forces for tooth movement. Participants will be instructed to wear the aligners intraorally for 10 days for a minimum of 22 hours per day. The aligners will be evaluated before use and after intraoral exposure to assess changes in mechanical properties and surface morphology.
Experimental: Triple-Layer TPU Aligner Group
Participants in this group will receive triple-layer thermoplastic polyurethane (TPU) MaxFlex aligners consisting of a soft inner layer, a rigid intermediate layer, and a flexible outer layer. The aligners will be worn intraorally for 10 days for a minimum of 22 hours per day. Aligners will be collected at baseline and after use for mechanical and surface analysis.
Triple-layer thermoplastic polyurethane (TPU) clear aligners composed of a multilayer structure including a soft inner layer, a rigid intermediate layer, and a flexible outer layer. These aligners are fabricated using thermoforming techniques and are designed to provide improved force delivery and adaptability. Participants will wear the aligners intraorally for 10 days for at least 22 hours per day. Pre- and post-use evaluations will be conducted to assess mechanical properties and surface morphology changes.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Effect of Oral Environment on Elastic Modulus of TPU Aligners
Prazo: Baseline (0 week) and after 2 weeks of intraoral use (minimum 22 hours/day)
This outcome measures the change in elastic modulus (MPa) of thermoplastic polyurethane (TPU) orthodontic aligners following intraoral exposure. Measurements are obtained using a dynamic mechanical analyzer and compared between single-layer and multilayer TPU aligners at baseline and after two weeks of clinical use to assess changes in stiffness and material integrity.
Baseline (0 week) and after 2 weeks of intraoral use (minimum 22 hours/day)
Effect of Oral Environment on Stress Relaxation of TPU Aligners
Prazo: Time Frame: Baseline (0 week) and after 2 weeks of intraoral use (minimum 22 hours/day)
This outcome measures the percentage stress relaxation (%) of TPU aligners following intraoral exposure. Stress decay over time is recorded using a dynamic mechanical analyzer and compared between single-layer and multilayer TPU aligners at baseline and after two weeks to evaluate force retention capacity.
Time Frame: Baseline (0 week) and after 2 weeks of intraoral use (minimum 22 hours/day)
Effect of Oral Environment on Creep Behavior of TPU Aligners
Prazo: Time Frame: Baseline (0 week) and after 2 weeks of intraoral use (minimum 22 hours/day)
This outcome measures creep (% strain) in TPU aligners under constant stress conditions using a dynamic mechanical analyzer. Comparisons are made between single-layer and multilayer TPU aligners at baseline and after two weeks to assess susceptibility to permanent deformation.
Time Frame: Baseline (0 week) and after 2 weeks of intraoral use (minimum 22 hours/day)

Colaboradores e Investigadores

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

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)

13 de setembro de 2025

Conclusão Primária (Real)

5 de março de 2026

Conclusão do estudo (Real)

16 de março de 2026

Datas de inscrição no estudo

Enviado pela primeira vez

19 de abril de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

27 de abril de 2026

Primeira postagem (Real)

5 de maio de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

5 de maio de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

27 de abril de 2026

Última verificação

1 de setembro de 2025

Mais Informações

Termos relacionados a este estudo

Termos MeSH relevantes adicionais

Outros números de identificação do estudo

  • TPU-ALIGNER-01
  • no identifier (Outro identificador: Akhtar Saeed Medical & Dental College)

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 .

Se inscrever