NCT06304129 · UNKNOWN

Diagnostic Performance of Plasma Biomarkers of Alzheimer's Disease Compared With CSF Markers

Sponsor: Central Hospital, Nancy, France

This study tests whether blood draws can match the accuracy of spinal fluid tests for detecting Alzheimer's-related changes in the brain. Researchers will compare blood levels of proteins like amyloid and tau against the standard lumbar puncture results in patients already being evaluated for Alzheimer's at a French hospital. This is a diagnostic accuracy study, not a drug trial — it is trying to validate a less invasive test, not treat anything.

You may qualify if

  • Man or woman aged 18 or over
  • Person affiliated to a social security scheme or beneficiary of such a scheme
  • Person who has received full information on the organization of the research and has signed an informed consent form
  • Person whose care requires a lumbar puncture to measure markers of Alzheimer's disease

You're excluded if

  • Adult subject to a legal protection measure (guardianship, curatorship, safeguard of justice)
  • An adult unable to give consent
  • Persons deprived of their liberty by judicial or administrative decision
  • Persons under psychiatric care under articles L. 3212-1 and L. 3213-1.
  • Pregnant, parturient or breast-feeding women
  • Persons staying in a health or social establishment for purposes other than research.

The sponsor's own eligibility wording, lightly reformatted. The study team makes the final eligibility decision — worth discussing with your doctor.

Eligibility criteria as of 2024-03-12

View full record on ClinicalTrials.gov

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