跳至主要内容
临床试验/NCT02884492
NCT02884492终止2 期

Imaging Tau in Alzheimer's Disease and Normal Aging

William Charles Kreisl1 个研究点 分布在 1 个国家目标入组 17 人开始时间: 2016年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
终止
发起方
入组人数
17
试验地点
1
主要终点
18F-THK-5351 Standardized Uptake Value Ratio

研究概览

简要总结

This study is being done to learn about tau tangles in Alzheimer's disease. A type of PET scan is used to measure the abnormal accumulation of protein called tau in the brain. These are thought to be involved in Alzheimer's disease. The investigators will also perform brain MRI and to tests to measure the participant's memory and thinking.

详细描述

This study is being done to determine the relationship between tau tangles and cognitive impairment in elderly subjects with different clinical and biomarker profiles of Alzheimer's disease (AD). Subjects will undergo screen that includes neuropsychological testing and brain MRI. This study uses a special type of scan called a PET scan to take pictures of the brain. During the PET scan, a special radioactive dye called 18F-THK-5351 is injected into the body. 18F-THK-5351 sticks to abnormal tangles made of the protein tau. Subjects will have the option to have lumbar puncture performed to measure CSF concentrations of biomarkers.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
50 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 50 and older.
  • Meet criteria for either a) amnestic mild cognitive impairment (single or mixed domain) or mild Alzheimer's disease, or b) have no cognitive impairment, based on history, exam, neuropsychological testing, and consensus diagnosis. MCI and mild AD patients must have Clinical Dementia Rating scale score of 0.5 or
  • Unimpaired subjects must have Clinical Dementia Rating scale score of
  • Subjects unable to provide informed consent must have a surrogate decision maker.
  • Written and oral fluency in English or Spanish.
  • Able to participate in all scheduled evaluations and to complete all required tests and procedures.
  • In the opinion of the investigator, the subject must be considered likely to comply with the study protocol and to have a high probability of completing the study.

排除标准

  • Past or present history of certain brain disorders other than MCI or AD.
  • Certain significant medical conditions, which make study procedures of the current study unsafe. Such serious medical conditions include uncontrolled epilepsy and multiple serious injuries.
  • Contraindication to MRI scanning.
  • Conditions precluding entry into the scanners (e.g. morbid obesity, claustrophobia, etc.).
  • History of kidney disease or presence of impaired kidney function based on laboratory tests at the screening visit.
  • History of liver disease or presence of impaired liver function based on laboratory tests at the screening visit.
  • Participation in the last year in a clinical trial for a disease-modifying drug for AD.
  • Inability to have a catheter in subject's vein for the injection of radioligand.
  • Inability to have blood drawn from subject's veins.

研究组 & 干预措施

Cognitive impairment

Experimental

Adults with Alzheimer's disease, preclinical Alzheimer's disease or impairment due to suspected non-Alzheimer's disease pathophysiology will receive 18F-THK- 5351 and/or lumbar puncture (optional).

干预措施: 18F-THK-5351 (Drug)

Cognitive impairment

Experimental

Adults with Alzheimer's disease, preclinical Alzheimer's disease or impairment due to suspected non-Alzheimer's disease pathophysiology will receive 18F-THK- 5351 and/or lumbar puncture (optional).

干预措施: Lumbar Puncture (optional) (Procedure)

No cognitive impairment

Active Comparator

Normal aging adults will receive 18F-THK- 5351 and/or lumbar puncture (optional).

干预措施: 18F-THK-5351 (Drug)

No cognitive impairment

Active Comparator

Normal aging adults will receive 18F-THK- 5351 and/or lumbar puncture (optional).

干预措施: Lumbar Puncture (optional) (Procedure)

结局指标

主要结局

18F-THK-5351 Standardized Uptake Value Ratio

时间窗: PET image data collected 50 min post-injection to 70 min post-injection of 18F-THK-5351

The standardize uptake value ratio is the concentration of radioactivity measured from the 18F-THK-5351 PET scan in the posterior cingulate gyrus, divided by that in the cerebellar gray matter (the reference region, which is expected to be devoid of tau pathology). This ratio is a relative measure of 18F-THK-5351 binding, and therefore of tau pathology, in brain tissue. PET image data was acquired from 50 min post-injection to 70 min post-injection of 18F-THK-5351.

次要结局

未报告次要终点

研究者

发起方
William Charles Kreisl
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

William Charles Kreisl

Principal Investigator

Columbia University

研究点 (1)

Loading locations...

相似试验

已完成
2 期
Imaging Tau in Alzheimer's Disease and Normal AgingAlzheimer Disease
NCT03373604Patrick Lao71
招募中
不适用
Molecular and Structural Imaging in Alzheimer's Disease: A Longitudinal StudyAmnestic SymptomsAtypical Alzheimer's DiseaseLogopenic Progressive Aphasia (LPA)Posterior Cortical Atrophy (PCA)Alzheimer DiseaseAlzheimer Disease, Early OnsetAmnestic DisorderAmnestic Mild Cognitive Disorder
NCT02740634Mayo Clinic60
已完成
1 期
Tau PET Imaging in Atypical DementiasPrimary Progressive Aphasia With Suspected Alzheimer's Disease
NCT03283449University of Chicago70
已完成
2 期
Tau Imaging in Tauopathies; Alzheimer's disease and Non-AD dementiasTauopathy1001462310012272dementia
NL-OMON50757Vrije Universiteit Medisch Centrum200
进行中(未招募)
1 期
Imaging of tau in patients with dementiaDementia inducing Alzheimer's disease, Frontotemporal dementia (FTD) and Lewy Body Dementia (DLB)MedDRA version: 20.0Level: PTClassification code 10012271Term: Dementia Alzheimer's typeSystem Organ Class: 10029205 - Nervous system disordersMedDRA version: 20.0Level: LLTClassification code 10057095Term: Diffuse Lewy body diseaseSystem Organ Class: 100000072901MedDRA version: 20.0Level: PTClassification code 10068968Term: Frontotemporal dementiaSystem Organ Class: 10029205 - Nervous system disordersMedDRA version: 20.0Level: LLTClassification code 10012283Term: Dementia due to other general medical conditionsSystem Organ Class: 100000014717
EUCTR2015-005604-29-NLVU University Medical Center