- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT02153255
Dynamic Gait Analysis in Children With Mucopolysaccharidosis Type IVa
Mucopolysaccharidosis Type IVa (MPS IVa, Morquio Disease) is a rare inherited lysosomal storage disorder caused by deficiency of the enzyme galactose-6-sulfatase.
Children with this disease accumulate a chemical called keratan sulphate, which stops their skeletons developing properly. They are very short in stature and many of their joints are unstable. Children with MPS IVa walk in a different way to other people due to a combination of lax ligaments and skeletal problems such as knock-knees.
Human walking involves the coordinated movements of all four limbs. As we walk, the arms swing oppositely to the legs. This movement pattern is very different in children with MPS IVa. This change seems to involve the whole musculoskeletal system and depends on the severity of the disease.
Recent studies in children with MPS IVa describing walking pattern have concentrated solely on the lower or upper limb respectively, and have not looked at the interaction of the upper and lower limbs during walking.
To our knowledge, the mechanics of walking in children with MPS IVa has not been investigated using a dynamic gait analysis tool (using cameras, sensors and electrodes to track the movements of different parts of the body during walking) and we aim to characterise this in a small number of children with MPS IVa and also examine the effects of splinting the wrist upon the walking pattern to see if this simple intervention makes it easier or more difficult for children with MPS IVa to walk.
Descripción general del estudio
Estado
Condiciones
Tipo de estudio
Contactos y Ubicaciones
Ubicaciones de estudio
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West Midlands
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Birmingham, West Midlands, Reino Unido, B4 6NH
- Birmingham Children's Hospital NHS Foundation Trust
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Método de muestreo
Población de estudio
Descripción
Inclusion Criteria:
- Confirmed diagnosis of MPS IVa (documented history of reduced leucocyte GALNS enzyme activity relative to the normal range of the laboratory performing the assay AND/OR molecular analysis showing two pathogenic mutations in the GALNS gene)
- Willing and able to provide written assent and parent/legal guardian able to provide written informed consent after the nature of the study has been explained and prior to any research-related procedures
- Between 6 and 18 years of age inclusive
- Willing to perform all study procedures as far as physically possible
Exclusion Criteria:
- Inability to comply with Gait Analysis protocol (e.g. nonambulant)
- Recent orthopaedic surgery that investigator deems might impact on Gait Analysis
- Use of any investigational product or investigational medical device other than BMN110 within 30 days prior to recruitment, or requirement for any investigational agent other than BMN110 prior to completion of all scheduled study assessments
- Concurrent disease or condition that would interfere with study participation or safety
- Any condition that, in the view of the Principal or Subinvestigators, places the subject at high risk of not completing the study procedures
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
Cohortes e Intervenciones
Grupo / Cohorte |
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Children With Mucopolysaccharidosis Type IVa
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Evidence of abnormal walking pattern and surface EMG activity as assessed by Dynamic Gait Analysis
Periodo de tiempo: Within 6 months of recruitment
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Assessment of head, trunk and joint positions during walking using a 12 camera Vicon motion analysis system.
Surface EMG analysis using a 16 channel wireless surface electromyographic (sEMG) system.
Assessment of lower limb joint moments and powers using Kistler 9281 and AMTI OPT 400600 force plates.
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Within 6 months of recruitment
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Change in gait pattern over one year
Periodo de tiempo: 12 months after first analysis
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Comparison of two gait analysis studies taken 12 months apart
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12 months after first analysis
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Effect on gait pattern of using wrist splints
Periodo de tiempo: Within 6 months of recruitment
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Assessment of repeat gait analysis measurements done at first visit whilst wearing wrist splints
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Within 6 months of recruitment
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Effect on gait pattern of lower limb surgery
Periodo de tiempo: Within 3 and 6 months of any lower limb surgery
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Further gait analysis studies will be done if a child undergoes any lower limb orthopaedic surgery during the study period and compared with pre-surgery analyses
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Within 3 and 6 months of any lower limb surgery
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Colaboradores e Investigadores
Colaboradores
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
Actualizaciones de registros de estudio
Última actualización publicada (Estimar)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
- Enfermedades metabólicas
- Enfermedades Genéticas Congénitas
- Enfermedades musculoesqueléticas
- Enfermedades del tejido conectivo
- Enfermedades óseas
- Metabolismo de carbohidratos, errores congénitos
- Metabolismo, errores congénitos
- Enfermedades de almacenamiento lisosomal
- Mucinosis
- Enfermedades óseas del desarrollo
- Mucopolisacaridosis
- Osteocondrodisplasias
- Mucopolisacaridosis IV
Otros números de identificación del estudio
- 14/WM/0120
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. .
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