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- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT02423850
Three-dimensional Measurements of Diabetic Foot Ulcers
Three-dimensional Measurements for Monitoring Wound Healing of Diabetic Foot Ulcers
Diabetic foot ulcers constitute an increasing health problem in Denmark concurrent with an ageing population and an increase in diabetes prevalence. Diabetic foot ulcers belong to the most serious and costly complications. Several studies have found that the size and depth of the ulcer is one of the major etiologic factors for delayed healing. Wound measurement is important in the monitoring of the wound healing process. For the last decade different 3D (three-dimensional) techniques for measuring wounds have been proposed in order to measure wound volume, but none of the technologies have been widely used. A 3D Wound Assessment Monitor (WAM) camera has been developed, which is able to measure wound size in 3D and to assess wound characteristics.
The investigators hypothesize that three-dimensional measurements of diabetic foot ulcers are feasible in the assessment of wound healing. A prospective cohort study is conducted in which newly admitted patients with a diabetic foot ulcer are included at the first visit at the multidisciplinary clinic. The patients are followed for one year or until complete wound healing, amputation or death. The four wound measurements: 2D area, 3D area, perimeter and volume are measured using the 3D-WAM camera with frequent intervals. Patient anthropometrics and wound data are collected during the study and correlated to the wound healing.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
Method
Newly admitted patients with a diabetic foot ulcer are included at the first visit in the multidisciplinary clinic. The data mentioned below are collected at the first visit and the following examinations are performed including 3D photos. The wound size (2D area, 3D area, perimeter and volume) are estimated from the photos using the 3D-WAM camera. The wound examination is repeated after 2, 4, 8, 12, 24, 36 and 52 weeks or until healing of the wound. The wound healing is estimated using changes in wound size per time unit. Patients are treated by standard ulcer treatment methods and are unaffected by the project per se. During the trial the different methods of treatment are noted including changes from initial treatment. The variables will be quantified after one year depending on time to heal, establishment of a chronic ulcer (non-healing after one year) or an amputation has been performed.
At baseline the following patient data will be collected:
- Demographic data: gender, age
- Smoking habits
- Time period between onset of wound to first visit in the multidisciplinary clinic
- Body Mass Index
- Comorbidity using Charlson Comorbidity Index score
- Type of diabetes, duration of diabetes
- Diabetic complications including retinopathy, albuminuria, coronary heart diseases and neuropathy
The following examinations will be performed at baseline:
- Blood pressure measurement
- Peripheral blood pressure
- Examination for neuropathy using monofilament
- Blood samples from patients with a diabetic foot ulcer
The clinical examination of the ulcer are performed at baseline and after 2, 4, 8, 12, 24, 36 and 52 weeks or until wound healing:
- Size of wound (2D area, 3D area, perimeter, volume) measured using the 3D-WAM camera
- Size of wound in 2D area using the digital imaging method with the software ImageJ
- Location of the ulcer
- Classification of ulcer: granulation, necrosis, epithelialisation
- Secretory potential
- Foot deformity
- Bone affection - if osteitis is suspected an x-ray is taken
- Signs of infection
The different types of ulcer treatment is registered for every ulcer:
- Type of bandage
- Antibiotics (local, systemic)
- Revision (method, frequency),
- Surgery
Effect variables
- Wound 2D area, 3D area, perimeter and volume
- Variation in 2D and 3D area measurements during the study period
- Percentage change in wound size after 2, 4, 8, 12, 24, 36 and 52 weeks
Endpoints
- Wound healing
- Amputations
- Chronic wound (non-healing after 1 year)
- Death
Significance
This project seeks to clarify whether 3D photos of wounds will provide accurate structural measures to illuminate the background for delayed ulcer healing, and thereby to create platform for a more evidence based treatment algorithm.
Tipo de estudio
Inscripción (Actual)
Contactos y Ubicaciones
Ubicaciones de estudio
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Odense, Dinamarca, 5000
- University Centre of Wound Healing, Odense University Hospital (OUH)
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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:
- Newly admitted patients with diabetic foot ulcers
- 18 years or older
Exclusion Criteria:
- Superficial wound (less than 5x5 mm with no substantial loss of subcutaneous tissue)
- Non-compliance (dementia, mental disorders)
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
Cohortes e Intervenciones
Grupo / Cohorte |
Intervención / Tratamiento |
---|---|
Diabetic foot ulcers
Newly referred patients with diabetic foot ulcers from the multidisciplinary clinic: University Centre for Wound healing, Odense University Hospital, Denmark.
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Three-dimensional wound measurement (2D area, 3D area, perimeter, volume) using 3D-WAM camera
Otros nombres:
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
Wound healing change quantified using the 3D-WAM camera
Periodo de tiempo: Photos are taken at week 0, 2, 4, 8, 12, 24, 36 and 52 weeks
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The 3D wound measurements at week 2, 4, 8, 12, 24, 36 and 52 are compared to the baseline measurement at week 0.
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Photos are taken at week 0, 2, 4, 8, 12, 24, 36 and 52 weeks
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Wound healing change quantified using digital imaging method
Periodo de tiempo: Photos are taken at week 0, 2, 4, 8, 12, 24, 36 and 52 weeks
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The 2D wound measurements at week 2, 4, 8, 12, 24, 36 and 52 are compared to the baseline measurement at week 0.
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Photos are taken at week 0, 2, 4, 8, 12, 24, 36 and 52 weeks
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
The variability in 2D area and 3D area measurements
Periodo de tiempo: Photos are taken at week 0, 2, 4, 8, 12, 24, 36 and 52 weeks
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The variability in 2D area (digital imaging method) and 3D area wound measurements (3D-WAM camera) at week 0, 2, 4, 8, 12, 24, 36 and 52 are compared
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Photos are taken at week 0, 2, 4, 8, 12, 24, 36 and 52 weeks
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Diabetes type is compared to outcome of the wound
Periodo de tiempo: Baseline until healing, amputation or chronic wound (52 weeks)
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Type 1 and 2
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Baseline until healing, amputation or chronic wound (52 weeks)
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Diabetes duration is compared to outcome of the wound
Periodo de tiempo: Baseline until healing, amputation or chronic wound (52 weeks)
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In years
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Baseline until healing, amputation or chronic wound (52 weeks)
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BMI (kg/m2) is compared to outcome of the wound
Periodo de tiempo: Baseline until healing, amputation or chronic wound (52 weeks)
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kg/m2
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Baseline until healing, amputation or chronic wound (52 weeks)
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Charlson index score is compared to outcome of the wound
Periodo de tiempo: Baseline until healing, amputation or chronic wound (52 weeks)
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In groups
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Baseline until healing, amputation or chronic wound (52 weeks)
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HbA1c is compared to outcome of the wound
Periodo de tiempo: Baseline until healing, amputation or chronic wound (52 weeks)
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mmol/mol
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Baseline until healing, amputation or chronic wound (52 weeks)
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Ischemia is compared to outcome of the wound
Periodo de tiempo: Baseline until healing, amputation or chronic wound (52 weeks)
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Ischemia is defined by ankle pressure below 70 mmHg and/or toe pressure below 45 mmHg
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Baseline until healing, amputation or chronic wound (52 weeks)
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Neuropathy is compared to outcome of the wound
Periodo de tiempo: Baseline until healing, amputation or chronic wound (52 weeks)
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Neuropathy is measured by Semmes Weinstein monofilament examination
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Baseline until healing, amputation or chronic wound (52 weeks)
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Wound duration is compared to outcome of the wound
Periodo de tiempo: Baseline until healing, amputation or chronic wound (52 weeks)
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In weeks
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Baseline until healing, amputation or chronic wound (52 weeks)
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Otras medidas de resultado
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
Quality of life (Questionaires) using 36-Item Short Form Survey (SF-36) is compared to outcome of the wound
Periodo de tiempo: Baseline, 24 and 52 weeks
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The higher the score the less disability
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Baseline, 24 and 52 weeks
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Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Knud Yderstræde, MD, PhD, Department of Endocrinology, Odense University Hospital
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
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 (Actual)
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 cardiovasculares
- Enfermedades Vasculares
- Trastornos del metabolismo de la glucosa
- Enfermedades metabólicas
- Enfermedades de la piel
- Enfermedades del sistema inmunológico
- Enfermedades autoinmunes
- Enfermedades del sistema endocrino
- Angiopatías diabéticas
- Úlcera en la pierna
- Úlcera de la piel
- Neuropatías diabéticas
- Enfermedades de los pies
- Diabetes mellitus
- Diabetes Mellitus, Tipo 2
- Pie diabético
- Úlcera del pie
- Diabetes Mellitus, Tipo 1
- Complicaciones de la diabetes
Otros números de identificación del estudio
- OUH3D02
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
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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