The Effect of Rapid and Slow Glucose Fall on the Subsequent Glucose Production in People With Type 1 Diabetes (RaSlo-19)
Descripción general del estudio
Estado
Estado
Condiciones
Condiciones
Intervención / Tratamiento
Intervención / Tratamiento
Tipo de estudio
Tipo de estudio
Inscripción (Actual)
Inscripción
Fase
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
-
-
-
Gentofte, Dinamarca, 2820
- Steno Diabetes Center Copenhagen
-
-
Criterios de participación
Criterio de elegibilidad
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Age 18-70 years
- Duration of Type 1 Diabetes ≥ 3 years
- Insulin pump use > 6 months
Exclusion Criteria:
- Use of anti-diabetic medicine (other than insulin), corticosteroids or other drugs affecting glucose metabolism during the study period or within 30 days prior to study start
- Allergy or intolerance to lactose or GlucaGen (Novo Nordisk, Bagsværd, DK)
- Use of medications that are known to cause QT interval prolongation
- Females who are pregnant, breast-feeding or intend to become pregnant or are not using adequate contraceptive methods
- Females who have different basal insulin pattern depending on their menstrual cycle
- Inability to understand the individual information and to give informed consent
- Current participation in another clinical trial that, in the judgment of the principle investigator, will compromise the results of the study or the safety of the subject
- Other concomitant medical or psychological condition that according to the investigator's assessment makes the individual unsuitable for study participation
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Ciencia básica
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación cruzada
- Enmascaramiento: Único
Número de brazos
Armas e Intervenciones
Grupo de participantes/brazoGrupo de participantes/brazo |
Intervención / TratamientoIntervención / Tratamiento |
|---|---|
|
Experimental: Rapid-Slow
This arm will begin with intervention "rapid" (rapid rate of fall in plasma glucose) for the first study visit and proceed to intervention "slow" (slow rate of fall in plasma glucose) for the second study visit.
|
Rapid lowering of plasma glucose using hypoglycemic clamp technique
Slow lowering of plasma glucose using hypoglycemic clamp technique
|
|
Experimental: Slow-Rapid
This arm will begin with intervention "slow" (slow rate of fall in plasma glucose) for the first study visit and proceed to intervention "rapid" (rapid rate of fall in plasma glucose) for the second study visit.
|
Rapid lowering of plasma glucose using hypoglycemic clamp technique
Slow lowering of plasma glucose using hypoglycemic clamp technique
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medidas de resultado primarias
Medida de resultado |
Periodo de tiempo |
|---|---|
|
Positive incremental area under the glucose curve (PI-AUC) (using the plasma glucose concentration before glucagon administration as basal level)
Periodo de tiempo: from 0-120 minutes after glucagon administration
|
from 0-120 minutes after glucagon administration
|
Medidas de resultado secundarias
Medidas de resultado secundarias
Medida de resultado |
Periodo de tiempo |
|---|---|
|
Total area under the glucose curve (AUC)
Periodo de tiempo: from 0-120 minutes after glucagon administration
|
from 0-120 minutes after glucagon administration
|
|
Peak plasma glucose
Periodo de tiempo: from 0-120 minutes after glucagon administration
|
from 0-120 minutes after glucagon administration
|
|
Incremental plasma glucose peak
Periodo de tiempo: from 0-120 minutes after glucagon administration
|
from 0-120 minutes after glucagon administration
|
|
Time-to-peak plasma glucose
Periodo de tiempo: from 0-120 minutes after glucagon administration
|
from 0-120 minutes after glucagon administration
|
|
Plasma glucose level
Periodo de tiempo: 120 minutes after glucagon administration
|
120 minutes after glucagon administration
|
|
Duration of plasma glucose above 4.0 mmol/l
Periodo de tiempo: from 0-120 minutes after glucagon administration
|
from 0-120 minutes after glucagon administration
|
|
Duration of plasma glucose above baseline
Periodo de tiempo: from 0-120 minutes after glucagon administration
|
from 0-120 minutes after glucagon administration
|
|
Number of subjects who, after reaching a plasma glucose value > 3.9 mmol/l following glucagon administration, maintain a plasma glucose level in the range of 3.9-10 mmol/l
Periodo de tiempo: throughout phase 4 (until 120 minutes after glucagon administration)
|
throughout phase 4 (until 120 minutes after glucagon administration)
|
|
Number of subjects who, after reaching a PG > 3.9 mmol/l following glucagon administration, maintain a plasma glucose level in the range of 3.9-7.8 mmol/l
Periodo de tiempo: throughout phase 4 (until 120 minutes after glucagon administration)
|
throughout phase 4 (until 120 minutes after glucagon administration)
|
|
Time from glucagon administration to reaching a plasma glucose level > 3,9 mmol/l
Periodo de tiempo: from 0-120 minutes after glucagon administration
|
from 0-120 minutes after glucagon administration
|
|
Duration of a plasma glucose level in the range of 3.9-10 mmol/l
Periodo de tiempo: from 0-120 minutes after glucagon administration
|
from 0-120 minutes after glucagon administration
|
|
Duration of a plasma glucose level in the range of 3.9-7.8 mmol/l
Periodo de tiempo: from 0-120 minutes after glucagon administration
|
from 0-120 minutes after glucagon administration
|
|
Change in insulin levels (measured as area under the curve)
Periodo de tiempo: 0-120 minutes after glucagon administration
|
0-120 minutes after glucagon administration
|
|
Change in insulin levels (measured as peak change)
Periodo de tiempo: from baseline to 120 minutes after glucagon administration
|
from baseline to 120 minutes after glucagon administration
|
|
Change in glucagon levels (measured as area under the curve)
Periodo de tiempo: 0-120 minutes after glucagon administration
|
0-120 minutes after glucagon administration
|
|
Change in glucagon levels (measured as peak change)
Periodo de tiempo: 0-120 minutes after glucagon administration
|
0-120 minutes after glucagon administration
|
|
Average changes in Edinburgh Hypoglycemia Scale
Periodo de tiempo: measured at baseline, 5 minutes prior to the end of phase 2, 5 minutes prior to the end of phase 3 and 30 and 115 minutes after glucagon administration
|
measured at baseline, 5 minutes prior to the end of phase 2, 5 minutes prior to the end of phase 3 and 30 and 115 minutes after glucagon administration
|
|
Average change in visual analogue scale score for nausea, headache, stomach ache and palpitations
Periodo de tiempo: measured at baseline, 5 minutes prior to the end of phase 2, 5 minutes prior to the end of phase 3 and 30 and 115 minutes after glucagon administration
|
measured at baseline, 5 minutes prior to the end of phase 2, 5 minutes prior to the end of phase 3 and 30 and 115 minutes after glucagon administration
|
|
Number of subjects experiencing vomiting
Periodo de tiempo: from 0-120 minutes after glucagon administration
|
from 0-120 minutes after glucagon administration
|
Colaboradores e Investigadores
Patrocinador
Patrocinador
Colaboradores
Colaboradores
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Inicio del estudio
Finalización primaria (Actual)
Finalización primaria
Finalización del estudio (Actual)
Finalización del estudio
Fechas de registro del estudio
Enviado por primera vez
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Publicado por primera vez
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización publicada
Última actualización enviada que cumplió con los criterios de control de calidad
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
Otros números de identificación del estudio
- H-19034585
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Tipo de información de apoyo para compartir IPD
- Protocolo de estudio
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.
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