- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT01959984
Study on the Comparison Between"Standard Noodles" and Traditional Carbohydrates in the Diagnosis of Diabetes Mellitus.
The object of this study is to compare "100g Standard Noodles " with traditional carbohydrates including 75g glucose solution in 300ml water and 100g steamed bread in the diagnosis of diabetes mellitus.
In this study, we will compare the different effects of "100g Standard Noodles Tolerance Test"and "75g Oral Glucose Tolerance Test"on plasma glucose, insulin, c- peptide level and the relevant hormones level including glucagon-like peptide-1( GLP-1) and glucagon. Besides, in part of the subjects, the difference between "100g Steamed Bread Tolerance Test", "100g Standard Noodles Tolerance Test" and "75g Oral Glucose Tolerance Test" will be further evaluated.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Anticipado)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
-
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Shanghai
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Shanghai, Shanghai, Porcelana, 200021
- Shanghai Jiao Tong University School of Medicine
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
Inclusion Criteria:
For healthy subjects:
- Between 16-70 years old.
- No weight fluctuation greater than 5% within 3 months.
- Understand and voluntarily sign an informed consent document prior to any study related assessments/procedures .
For subjects with impaired glucose regulation(IGR):
- Between 16-70 years old.
- Impaired fasting glucose(IFG):6.1mM(109mg/ml)≤fasting plasma glucose(FPG)<7.0mM(126mg/ml),or impaired glucose tolerance(IGT):7.8mM(140mg/ml)≤2h plasma glucose(2hPG)<11.1mM(200mg/dl),or both.
- No weight fluctuation greater than 5% within3 months.
- Keep stable antidiabetic therapy for at least 2 months.
- Understand and voluntarily sign an informed consent document prior to any study related assessments/procedures .
For subjects with type 2 diabetes mellitus(T2DM):
- Between 16-70 years old.
- T2DM:diabetic symptoms plus random blood glucose(RBG)≥11.1mM,or FPG ≥7.0mM(126mg/dl),or 2hPG ≥11.1mM(200mg/dl).
- No weight fluctuation greater than 5% within 3 months.
- Keep stable antidiabetic therapy at least for 2 months.
- Understand and voluntarily sign an informed consent document prior to any study related assessments/procedures.
For subjects with type 1 diabetes mellitus(T1DM):
- Between 16-70 years old.
- T1DM:diabetic symptoms plus RBG≥11.1mM,or FPG ≥7.0mM(126mg/dl),or 2hPG ≥11.1mM(200mg/dl).
- Present at least one positive antibody of β cell including ICA,IAA,GADA,IA-2A and IA-2βA.
- No weight fluctuation greater than 5% within 3 months.
- Keep stable antidiabetic therapy for at least 2 months.
- Understand and voluntarily sign an informed consent document prior to any study related assessments/procedures.
Exclusion Criteria:
For healthy subjects:
- Be diagnosed with diabetes or IGR in late 3 months.
- With any significant medical condition,laboratory abnormality,or psychiatric disorders that will prevent the subject from participating in the study.
- Any medical or surgical conditions possibly affecting the experiment result.
- Participated in a clinical study involving administration of medication within 90 days.
- Donated blood or plasma or had any other significant blood loss within 2 months.
- Any clinically significant allergic diseases.
- Recently drug or alcohol abuse(>35unit/week,1unit=8 g alcohol@1 standard drink@250ml beer@140ml wine@25ml strong alcohol drink like whiskey.)
- Smokers or users of other tobacco products in the 3 months prior to screening.
For IGR and DM:
- History of pancreatic diseases such as pancreatic cancer or pancreatitis.
- Suffered from acute complications such as diabetic ketoacidosis and hyperosmolar coma within 3 months.
- With any significant medical condition,laboratory abnormality,or psychiatric disorders that will prevent the subject from participating in the study.
- Malignant tumor.
- Being allergic to experiment arms.
- Recently drug or alcohol abuse(>35unit/week,1unit=8 g alcohol@1 standard drink@250ml beer@140ml wine@25ml strong alcohol drink like whiskey.)
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación cruzada
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
---|---|
Experimental: 100g Standard Noodles
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Subjects are required to take 100g standard noodles,and then blood samples are collected at 0min,30min,60min,120min,180min.
|
Experimental: 75g Oral Glucose
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Subjects are required to take 75g glucose solution,and then blood samples are collected at 0min,30min,60min,120min,180min.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
The plasma glucose level.
Periodo de tiempo: 12 months
|
The primary outcome measures the plasma glucose level at 0min,30min,60min,120min,180min during "75g Oral Glucose Tolerance Test" and "100g Standard Noodles Tolerance Test" .
|
12 months
|
The insulin level.
Periodo de tiempo: 12 months
|
The primary outcome measures the insulin level at 0min,30min,60min,120min,180min during "75g Oral Glucose Tolerance Test" and "100g Standard Noodles Tolerance Test" .
|
12 months
|
The c-peptide level.
Periodo de tiempo: 12 months
|
The primary outcome measures the c-peptide level at 0min,30min,60min,120min,180min during "75g Oral Glucose Tolerance Test" and "100g Standard Noodles Tolerance Test" .
|
12 months
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
The GLP-1 level.
Periodo de tiempo: 12months
|
The outcome measures of the GLP-1 level at 0min,30min,60min,120min,180min during "75g Oral Glucose Tolerance Test" and "100g Standard Noodles Tolerance Test" .
|
12months
|
The Glucagon level.
Periodo de tiempo: 12 months
|
The outcome measures of the glucagon level at 0min,30min,60min,120min,180min during "75g Oral Glucose Tolerance Test" and "100g Standard Noodles Tolerance Test" .
|
12 months
|
The other relevant incretin hormones levels.
Periodo de tiempo: 12 months
|
The outcome measures of the relevant incretin hormones level at 0min,30min,60min,120min,180min during "75g Oral Glucose Tolerance Test" and "100g Standard Noodles Tolerance Test" .
|
12 months
|
The plasma glucose, insulin, c-peptide and relevant incretin hormones level during "75g Oral Glucose Tolerance Test", "100g Standard Noodles Tolerance Test" and "100g Steamed Bread Tolerance Test".
Periodo de tiempo: 12 months
|
12 months
|
Otras medidas de resultado
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
Safety
Periodo de tiempo: 12 months
|
Document the frequency and extent of side-effects.
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12 months
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Guang Ning, MD,PHD, Shanghai Jiao Tong University School of Medicine
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Finalización primaria (Anticipado)
Finalización del estudio (Anticipado)
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
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- CCEMD018
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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