- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07659041
Effectiveness, Patient Acceptance, and Cost Estimation of 3D-printed Retainer Compared to Hawley Retainer in Expansion Case: a Randomized Controlled Trial
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
Tipo de estudio
Inscripción (Estimado)
Fase
- No aplica
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Asma Ashari, BDS Adel, MClinDent Lon, MOrth
- Número de teléfono: +603 8921 5555
- Correo electrónico: asmaashari@ukm.edu.my
Copia de seguridad de contactos de estudio
- Nombre: ALIZAE MARNY FADZLIN SYED MOHAMED
- Número de teléfono: +6038921 5555
- Correo electrónico: alizaemarny@ukm.edu.my
Ubicaciones de estudio
-
-
Kuala Lumpur
-
Kuala Lumpur, Kuala Lumpur, Malasia, 50300
- National University of Malaysia
-
Contacto:
- Fakulti pergigian UKM
- Número de teléfono: +6039289 7741
- Correo electrónico: asmaashari@ukm.edu.my
-
Investigador principal:
- Mei Ling Cheng
-
Kuala Lumpur, Kuala Lumpur, Malasia, 50603
- University Malaya
-
Contacto:
- May Nak Lau
- Número de teléfono: +60379674802
- Correo electrónico: minalau@um.edu.my
-
Sub-Investigador:
- Zhang Yi Tan
-
-
Selangor
-
Sungai Buloh, Selangor, Malasia, 47000
- University Teknologi Mara Selangor branch
-
Contacto:
- Nik Mukhriz Nik Mustapha
- Número de teléfono: +6036126 6103
- Correo electrónico: nikmukhriz@uitm.edu.my
-
Sub-Investigador:
- Siti Nor Hafizah Salehun
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Niño
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Patients aged 16 years or older at the time of debonding
- Treatment plan of extraction or non-extraction followed by straight wire appliances in the upper arch only or both arches
- Undergone expansion treatment in the upper arch causing an arch width increase of 3-10mm, either using a Quadhelix, expansion with archwires, or URA with midline screw
- Had pretreatment dental cast
- Had no chronic medical condition.
Exclusion Criteria:
- Cleft lip and palate
- Chronic medical conditions
- Broken teeth or bubbles on study model at site of measurement.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Otro
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Comparador activo: Hawley retainer
A screening will be done to select suitable patients for the study.
Only patients who fulfil the criteria will be invited to participate in this study.
Following informed consent, eligible subjects will be randomly allocated into one of two groups wither hawley retainer or 3D printed retainer.
Fabrication of Hawley retainers will be done using a standardized design across all centres.
|
Hawley retainers have served as the established standard for retention after maxillary expansion.
Standard design of Hawley Retainer: - Labial bow (0.8mm hard stainless steel) from canine to canine - Adam clasp on the molar (0.7mm hard stainless steel) - acrylic baseplate (2-3mm thickness) .
|
|
Experimental: 3D printed retainer
A screening will be done to select suitable patients for the study.
Only patients who fulfil the criteria will be invited to participate in this study.
Following informed consent, eligible subjects will be randomly allocated into one of two groups wither hawley retainer or 3D printed retainer.
Fabrication of 3d printed retainers will be done using a standardized design at one main centres by one technician using Nextdent Orhtoflex Resin.
|
3D-printed retainer Using Nextdent Orthoflex resin Standard design of 3D printed retainer:
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Retention of the maxillary expansion
Periodo de tiempo: 12 months
|
|
12 months
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Patient acceptance
Periodo de tiempo: 12 months
|
Subjects will be given and asked to complete a questionnaire on patient acceptance (see attachment) at 6 and 12 months post-debond. The Questionnaire has been validated and published by (Saw et al. 2025). It uses a Visual Analogue Scale (VAS) to ask six questions related to subject acceptance of orthodontic retainers in fitting, speech, appearance, oral hygiene, durability, and comfort. Refer to Attachment 1 (Malay version) and Attachment 2 (English Version) for the questionnaires. |
12 months
|
|
cost estimation
Periodo de tiempo: 6 months
|
To estimate and compare the costs associated with the implementation and provision of 3D-printed retainers between clinics with existing in-house 3D-printing facilities and clinics planning to acquire 3D-printing services.
The analysis will include direct costs such as equipment acquisition, materials, software, maintenance, laboratory procedures, and staff chairside time.
|
6 months
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Director de estudio: Asma Ashari, MClinDent Lon, National University of Malaysia
Publicaciones y enlaces útiles
Publicaciones Generales
- Hichens L, Rowland H, Williams A, Hollinghurst S, Ewings P, Clark S, Ireland A, Sandy J. Cost-effectiveness and patient satisfaction: Hawley and vacuum-formed retainers. Eur J Orthod. 2007 Aug;29(4):372-8. doi: 10.1093/ejo/cjm039.
- Naeem OA, Bencharit S, Yang IH, Stilianoudakis SC, Carrico C, Tufekci E. Comparison of 3-dimensional printing technologies on the precision, trueness, and accuracy of printed retainers. Am J Orthod Dentofacial Orthop. 2022 Apr;161(4):582-591. doi: 10.1016/j.ajodo.2021.03.016.
- Firlej M, Zaborowicz K, Zaborowicz M, Firlej E, Domagala I, Pieniak D, Igielska-Kalwat J, Dmowski A, Biedziak B. Mechanical Properties of 3D Printed Orthodontic Retainers. Int J Environ Res Public Health. 2022 May 9;19(9):5775. doi: 10.3390/ijerph19095775.
- Tsoukala E, Lyros I, Tsolakis AI, Maroulakos MP, Tsolakis IA. Direct 3D-Printed Orthodontic Retainers. A Systematic Review. Children (Basel). 2023 Apr 3;10(4):676. doi: 10.3390/children10040676.
- Saw ZK, Yuen JJX, Ashari A, Ibrahim Bahemia F, Low YX, Nik Mustapha NM, Lau MN. Forward-backward translation, content validity, face validity, construct validity, criterion validity, test-retest reliability, and internal consistency of a questionnaire on patient acceptance of orthodontic retainer. PLoS One. 2025 Jan 3;20(1):e0314853. doi: 10.1371/journal.pone.0314853. eCollection 2025.
- Nakornnoi T, Bunjerdjin P, Santiwong P, Sipiyaruk K, Neoh SP, Chintavalakorn R. The Influence of Thickness on the Mechanical Behaviors of 3D Printing Resins for Orthodontic Retainers. Int J Biomater. 2024 Jun 25;2024:7398478. doi: 10.1155/2024/7398478. eCollection 2024.
- Ashari A, Xian L, Syed Mohamed AMF, Wahab RMA, Kit YC, Tata MD, Sinnasamy S, Kuppusamy E. One-year comparative assessment of retention of arch width increases between modified vacuum-formed and Hawley retainers. Angle Orthod. 2022 Mar 1;92(2):197-203. doi: 10.2319/050921-363.1.
- Ashari A, Nik Mustapha NM, Yuen JJX, Saw ZK, Lau MN, Xian L, Syed Mohamed AMF, Megat Abdul Wahab R, Yeoh CK, Deva Tata M, Sinnasamy S. A two-year comparative assessment of retention of arch width increases between modified vacuum-formed and Hawley retainers: a multi-center randomized clinical trial. Prog Orthod. 2022 Aug 26;23(1):40. doi: 10.1186/s40510-022-00424-5.
- Stoev YY, Uzunov TT, Stoyanova NS, Grozdanova-Uzunova RG, Kosturkov DN, Taneva IK. Mechanical properties of materials for 3D printed orthodontic retainers. Folia Med (Plovdiv). 2023 Dec 31;65(6):986-992. doi: 10.3897/folmed.65.e107299.
- Neoh SP, Khantachawana A, Chintavalakorn R, Santiwong P, Srikhirin T. Comparison of physical, mechanical, and optical properties between thermoplastic materials and 3-dimensional printing resins for orthodontic clear retainers. Am J Orthod Dentofacial Orthop. 2025 Jan;167(1):95-109.e1. doi: 10.1016/j.ajodo.2024.06.010.
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Otros números de identificación del estudio
- JEP 2025-630 (Otro identificador: National university of Malaysia)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Descripción del plan IPD
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .