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M2 Receptor Measurements in Aging and in Alzheimer's Disease

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Qué se está recopilando

Datos de Medicamento

+ drug Data

Medicamento
Quiénes están siendo reclutados

Trastornos Mentales+3

+ Enfermedades del Cerebro

+ Enfermedades del Sistema Nervioso Central

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Cómo está diseñado el estudio

Observacional
Inicio del estudio: abril de 1999
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Resumen

Patrocinador PrincipalNational Institute of Mental Health (NIMH)
Última actualización: 4 de marzo de 2008
Extraido de una base de datos validada por el gobierno.Reclamar como socio

Fecha de inicio: 1 de abril de 1999

Fecha en la que se inscribió al primer participante.

The Geriatric Psychiatry Branch (GPB) of the National Institute of Mental Health (NIMH) proposes to study the effect of aging and Alzheimer's Disease (AD) on muscarinic type 2 (M2) receptor density and function using the ligand [F-18] FP-TZTP. M2 receptors are primarily autoreceptors found on acetylcholine (ACh) neurons, and are lost along with ACh neurons in aging and AD, particularly in the cerebral cortex. As we near completion of the study of the young versus the old, we would like to add a few more healthy subjects to achieve better gender balance, continue the accrual of Alzheimer's patients and expand the Protocol to include its natural scientific progression. Quantification of M2 receptors with a single FP-TZTP scan as we are currently performing with 99-M-0073 provides a measure of the number of cholinergic receptors in the brain, but not their capacity to release acetylcholine into the synapse. To test this capacity requires a second TZTP scan and the use of an agent that alters acetylcholine concentrations in the synapse. Non-human primate studies performed here (1) have found PET scans with FP-TZTP to be sensitive to changes in acetylcholine synapse concentrations, as a result of competition, in response to the adminstration of the acetylinesterase inhibitor physostigmine. We would like to use physostigmine in all groups; young, older normal, and Alzheimer's patients to infer differences in capacity to release acetylcholine.

NCT00001917
Patrocinador PrincipalNational Institute of Mental Health (NIMH)
Última actualización: 4 de marzo de 2008
Extraido de una base de datos validada por el gobierno.Reclamar como socio

Protocolo

Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.
Detalles del Diseño

Se reclutarán 150 pacientes

Número total de participantes que el ensayo clínico espera reclutar.

Elegibilidad

Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.
Condiciones
Criterios

Cualquier sexo

Sexo biológico de los participantes elegibles para inscribirse.

Voluntarios sanos permitidos

Indica si personas sanas, sin la condición que se estudia, pueden participar.

Condiciones

Patología

Trastornos MentalesEnfermedades del CerebroEnfermedades del Sistema Nervioso CentralDemenciaEnfermedades del sistema nerviosoEnfermedad de Alzheimer

Criterios

INCLUSION CRITERIA: Healthy males and females between 20-100 years old and volunteers with AD. AD volunteers must meet the NINCDS-ADRDA criteria for possible, probable, or definite AD. All subjects will be required to be off all prescription medications which could effect the PET scan, such as medications with anticholinergic effects, for two weeks to one month prior to the PET scan, and off psychotropic medication for one month. Subjects will be cautioned not to consume alcohol, marijuana, or psychotropic drugs while on the study, nor to smoke, use caffeinated beverages, or take over-the-counter medications such as cold medications (ie: Benadryl, Sudafed) for at least 12 hours prior to the PET scan. EXCLUSION CRITERIA: Patients withe significant cardiovascular disease, history of alcoholism, significant head trauma, uncontrolled hypertension, diabetes, bleeding disorders or other medical conditions which would make it medically unsafe to perform any part of the PET scan or would confound data analysis. Subjects with evidence of significant chronic disease to be accepted into the healthy control group. Subjects must not be pregnant.

Centros del Estudio

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National Institute of Mental Health (NIMH)

Bethesda, United StatesAbrir National Institute of Mental Health (NIMH) en Google Maps
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