Actively Recruiting
Analysis of Clinical Data and Diagnosis in People Undergoing Alzheimer Biomarker Testing in Cerebrospinal Fluid
Led by University Hospital, Strasbourg, France · Updated on 2023-04-27
10000
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Cognitive neurodegenerative diseases, such as Alzheimer's disease and other dementias, pose significant public health challenges due to difficulties in making accurate diagnoses during a patient's lifetime. This research aims to better understand how biomarkers found in cerebrospinal fluid (CSF) can improve diagnosis accuracy for these diseases, which often share overlapping symptoms and progress slowly over many years. The study also seeks to identify biomarkers specific to different neurodegenerative conditions to aid in their diagnosis. Participants with cognitive disorders who undergo a lumbar puncture as part of their diagnostic process at the memory center are observed in this study. The lumbar puncture procedure collects cerebrospinal fluid, which is analyzed for Alzheimer's disease biomarkers and potentially others related to different neurodegenerative diseases. This observational study includes patients with various cognitive impairments who are monitored without altering their standard clinical care. During the study, researchers collect and analyze cerebrospinal fluid samples over a one-year period. They also work on establishing new clinical study collaborations within the same timeframe. The study involves reviewing clinical data and diagnosis information to improve understanding of biomarker use in neurodegenerative disease diagnosis. Participant involvement includes routine lumbar puncture procedures and clinical assessments as part of their healthcare, with data collected for research purposes.
CONDITIONS
Brief Title
Cerebro Spinal Fluid Collection (CSF)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients undergoing lumbar puncture
- Patients with an accurate clinical diagnosis
You will not qualify if you...
- Patients who have not had a lumbar puncture
- Patients without accurate diagnostic information
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 1 year
Participants undergo lumbar puncture to collect cerebrospinal fluid as part of their diagnostic process for cognitive impairment.
1 lumbar puncture visit
Duration - Up to 1 year
Participants are observed following lumbar puncture to analyze clinical data and diagnosis outcomes related to Alzheimer biomarkers.
Periodic visits depending on clinical follow-up
Trial Site Locations
Total: 1 location
1
Service d'évaluation et Centre Mémoire de Ressources et de Recherche (CM2R), Hôpital de jour Saint François - Pôle de Gériatrie, Hôpitaux Universitaires de Strasbourg, Hôpital de la Robertsau
Strasbourg, France, 67091
Actively Recruiting
Research Team
F
Frédéric BLANC, MD/PhD
O
Olivier BOUSIGES, PharmD/PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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