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Brain Tissue Collection for Neuropathological Studies

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Ce qui est collecté

Collecte de données

Qui peut participer

Bipolar Disorder
+3

+ Depression
+ Anxiety Disorders
Comment se déroule l'étude

Autre

Observationnel
Date de début : mai 1990

Résumé

Sponsor principalNational Institute of Mental Health (NIMH)
Dernière mise à jour : 9 décembre 2019
Issu d'une base de données validée par les autorités. Revendiquer cette étude
Date de début de l'étude : 29 mai 1990Date à laquelle le premier participant a commencé l'étude.

The purpose of this study is to collect and study the brain tissue of deceased individuals to learn more about the nervous system and mental disorders. Information gained from donated tissue may lead to better treatments and potential cures for nervous system and mental disorders. This study will ask relatives of deceased individuals to donate the brains of their deceased relatives to allow further study of neurological and psychiatric disorders. We do not accept prospective donations. The knowledge of how affected tissue deviates from normal control tissue is an integral part of fully understanding a neurological or psychiatric disorder. The purpose of this protocol is to establish a coordinating program with the Office of the Chief Medical Examiner in Washington, DC, the Virginia Office of the Chief Medical Examiner, Central District, and Virginia the Office of the Chief Medical Examiner, Northern District for the donation of brain tissue. Dissected brain tissue from selected brain regions, including but not limited to the dorsolateral prefrontal cortex and hippocampal formation, will be assembled from large cohorts of normal controls and schizophrenic subjects. The expression of mRNA and protein for selected molecules, chosen on the basis of their genetic association with schizophrenia, will be measured with a variety of assays including but not limited to qPCR and Western blots. Outcome measures are the statistical comparison within normal controls of mRNA and/or protein levels in groups segmented by genotype. Similar comparisons will be made between schizophrenic cohorts and normal controls, in a diagnosis by genotype analysis with an ANOVA, or when appropriate an ANCOVA (controlling for variables such as age, race, gender, and postmortem interval).

Titre officielBrain Procurement for the Human Brain Collection Core 
Sponsor principalNational Institute of Mental Health (NIMH)
Dernière mise à jour : 9 décembre 2019
Issu d'une base de données validée par les autorités. Revendiquer cette étude

Protocole

Cette section fournit des détails sur le plan de l'étude, y compris la manière dont l'étude est conçue et ce qu'elle évalue.
Détails du design
2161 participants à inclureNombre total de participants que l'essai clinique vise à recruter.

Éligibilité

Les chercheurs recherchent des patients correspondant à une certaine description appelée critères d'éligibilité : état de santé général ou traitements antérieurs du patient.
Conditions
Critères
Tout sexeLe sexe biologique des participants éligibles à s'inscrire.
Volontaires sains autorisésIndique si les individus en bonne santé et ne présentant pas la condition étudiée peuvent participer.
Conditions
Pathologie
Bipolar Disorder
Depression
Anxiety Disorders
Schizophrenia
Tourette's Syndrome
Brain Diseases
Critères

* INCLUSION CRITERIA: Brain tissue is needed from individuals suffering from a variety of neuropsychiatric disorders, especially schizophrenia, but also anxiety disorders, suicide, bipolar disorder, depression, Tourette's Syndrome, drug addictions (PCP, cocaine, alcohol, heroin or the like) and any form of dementia. In addition, brains from normal individuals without a history of neuropsychiatric disease will be needed for controls. EXCLUSION CRITERIA: No living subjects are enrolled in this protocol. Tissue is obtained after death, with the permission of next of kin, or from existing institutions with appropriate samples via an MTA or other applicable agreement. Brain tissue is excluded from collection if there is a previously known history of strokes, lesions, or other major neuropathological abnormalities prior to the consenting process.



Centres d'étude

Ce sont les hôpitaux, cliniques ou centres de recherche où l'essai est conduit. Vous pouvez trouver le site le plus proche de vous ainsi que son statut.
Cette étude comporte 3 sites
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Office of the Chief Medical ExaminerWashington, United StatesVoir le site
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National Institutes of Health Clinical Center, 9000 Rockville PikeBethesda, United States
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Office of the Chief Medical ExaminerFairfax, United States

Suspendu3 Centres d'Étude