German Dementia Registry - GDR

Klinik für Neurologie des Uniklinikums Aachen0 个研究点目标入组 500 人开始时间: 2022年4月1日最近更新: 2024年8月19日

适应症

试验速览

暂无简介。

•Ability of the participant and/or his/her legally authorized representative (e.g., spouse or legal guardian), as appropriate and applicable, to understand the purpose and risks of the register and provide signed and dated informed consent and authorization to use protected health information (PHI) in accordance with national and local privacy regulations.
•Participating patients must have a diagnosis of SCI, MCI, early dementia, moderate dementia or severe dementia of different etiology (i.e. Alzheimer’s Disease, Frontotemporal Dementia, Parkinson’s Disease, Lewy-Body Dementia, Progressive Supranuclear Palsy, Corticobasal Degeneration, Normal Pressure Hydrocephalus, Major Depression; Vascular Dementia; TDP-43 associated limbic encephalopathy (LATE), Mixed Dementia AD + VaD, Prion-Associated Dementia) with fluid and/or imaging biomarkers.
•At least 18 years of age.
•Inclusion Criteria for familiy member:
•At least 18 years of age.
•Patient was included in the registry
•Family member is strongly involved to the patient's life according to the patient’s statement
•Ability of the participant, as appropriate and applicable, to understand the purpose and risks of the register

•Unable or unwilling to provide informed consent.
•No available biomarkers such as cerebrospinal fluids (CSF) amyloid beta 1-42, amyloid beta 1-40, amyloid beta 1-42/amyloid beta 1-40 ratio, total tau and phospho-tau, amyloid or tau imaging.

发起方

Klinik für Neurologie des Uniklinikums Aachen