Actively Recruiting

All Genders
ID04844060

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

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients undergoing lumbar puncture
  • Patients with an accurate clinical diagnosis
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

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

Long-term Monitoring

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

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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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