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临床试验/NCT06244875
NCT06244875尚未招募不适用

Collection Biologique Des Atteintes Neurocognitives

Assistance Publique - Hôpitaux de Paris0 个研究点目标入组 3,000 人开始时间: 2024年2月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
3,000
主要终点
Identification of new biomarkers for neurodegenerative diseases

研究概览

简要总结

The development of biological biomarkers reflecting neuropathology has enhanced the diagnostic precision of Alzheimer's disease over the past decade, compared to the clinical diagnosis that suffers from low specificity. Patients undergoing evaluation in specialized memory clinics suspected of major or minor neurocognitive disorder are notably examined through a lumbar puncture to measure beta-amyloid 42, beta-amyloid 40, total tau, and phosphorylated tau in the cerebrospinal fluid (CSF). The purpose of this clinico-biological collection is to better characterize the existing biomarkers used in clinical practice, as well as the development of new diagnostic or prognostic biomarkers for neurodegenerative diseases causing neurocognitive disorder (Alzheimer's disease, Lewy body disease, frontotemporal lobar degeneration, in particular).

The primary objective is to gain a better understanding of conventional biomarkers and to develop new diagnostic and prognostic biomarkers for neurocognitive diseases: establishing a prospective clinico-biological collection of patients evaluated in clinical practice for a neurocognitive disorder.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult patient
  • Not under legal guardianship
  • Clinical indication for blood and cerebrospinal fluid (CSF) biomarkers measurement during a day hospital stay for Alzheimer's disease (beta-amyloid peptide, tau protein).
  • Signature of the research consent form.

排除标准

  • Not affiliated with a social security scheme.
  • Patient under State Medical Aid (AME).

结局指标

主要结局

Identification of new biomarkers for neurodegenerative diseases

时间窗: Up to 10 years

次要结局

  • Description of the level of usual biomarkers by type of dementia(Up to 10 years)
  • Evaluation of the relationship between biomarker levels and cognitive evolution measured in routine care(Up to 10 years)
  • Comparison of biomarker levels in neurodegenerative pathologies and psychiatric pathologies with cognitive expression(Up to 10 years)

研究者

申办方类型
Other
责任方
Sponsor

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