- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT01792453
240 mL Water Drink Study
MRI Quantification of Gastric and Small Bowel Liquid Volumes Before and After Ingestion of the Standard Oral Solid Delivery 240 mL Water Drink
Descripción general del estudio
Descripción detallada
Solid oral delivery is the most frequently used route of administration for pharmaceutical drug products. Along with other important physiological parameters, the volume of liquid in the small intestine (SILV) has the potential to greatly influence the rate and extent of drug dissolution and absorption in the GI tract, or "oral bioperformance". Modeled small bowel absorption of a drug can vary by more than five-fold as SILV decreases from 500 to 50 ml. To obtain reasonable predictions of oral bioperformance scientists must design meaningful in vitro dissolution tests and mechanistic drug transport models that capture the range of SILV in humans. However, little is known about liquid volumes in the gut, mostly due to invasiveness of previous techniques. A recent study has drawn great attention to the possibility of the liquid in the small intestine existing in discrete liquid "pockets" hence it would also be desirable to monitor the time courses and volumes of individual water pockets in the small intestine.
Magnetic resonance imaging (MRI) is the ideal tool to carry out serial and non-invasive imaging of gastrointestinal function. MRI is inherently suited to image liquid materials and this ability has been exploited to image liquids in the undisturbed gastrointestinal tract. Gastric emptying measurements have been long established and validated. Small bowel liquid volumes measurements have been recently validated against naso-duodenal infusion. Ultimately, the findings with this study will provide novel insights on the volume and distribution of ingested liquids in the gastrointestinal tract.
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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Nottingham, Reino Unido, NG7 2RD
- University of Nottingham
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Apparently healthy; no medical conditions that might affect the study measurements
- Male or female
- Age between 18 and 55 years of age
- Body mass index (BMI) between 18.5 and 24.9 kg m-2
- Suitable for MRI scanning (eg absence of metal implants, infusion pumps and pacemakers as assessed by the MRI safety questionnaire
Exclusion Criteria:
- Previous gastrointestinal surgery (excluding cholecystectomy and appendectomy)
- Known gastrointestinal disease
- Smoking
- History of alcohol or drug abuse
- Taking medication that is likely to affect gastrointestinal function
- Participation in night shift work the week prior to the study day. (Night work is defined as working between midnight and 6 am)
- Strenuous exercise greater than 10 hours per week
- Consumption of more than 21 units of alcohol in a typical week
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Ciencia básica
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: 240 mL water drink
Volunteers will be asked to drink 240 mL water drink
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Time course of small bowel liquid volume after ingesting 240 mL of water
Periodo de tiempo: 0 - 120 mins
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Time course for the volume of freely mobile water in the small bowel over 2 hours
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0 - 120 mins
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Time course of gastric liquid volume after ingesting 240 mL of water
Periodo de tiempo: 0 - 120 mins
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Gastric volumes obtained from MRI as a function of time
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0 - 120 mins
|
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Number of liquid pockets in the small bowel
Periodo de tiempo: 0 - 120 mins
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Assessment of the number of pockets of liquid in the small bowel as seen on the MR images
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0 - 120 mins
|
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Volume of liquid pockets in the small bowel
Periodo de tiempo: 0 - 120 mins
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The volume of freely mobile liquid in each of the liquid pockets identified on the MR image
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0 - 120 mins
|
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Summary information on the location of liquid pockets by quadrant
Periodo de tiempo: 0 - 120 mins
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Details on the distribution of the liquid pockets as seen on the MR images
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0 - 120 mins
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Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Kathryn Murray, PhD, University of Nottingham
- Investigador principal: Caroline Hoad, PhD, University of Nottingham
- Investigador principal: Penny Gowland, PhD, University of Nottingham
- Investigador principal: Susan Pritchard, MSc, University of Nottingham
- Investigador principal: Martin Garnett, University of Nottingham
- Investigador principal: Robin Spiller, FRCP, University of Nottingham
- Investigador principal: Gregory Amidon, University of Michigan
- Investigador principal: Gordon Amidon, University of Michigan
- Investigador principal: Deanna Mudie, University of Michigan
- Director de estudio: Luca Marciani, PhD, University of Nottingham
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
Otros números de identificación del estudio
- A10012013
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. .