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Cerebrospinal Fluid Collection and Repository Storage

Cerebrospinal Fluid Collection and Repository Storage

Non Recruiting
2-110 years
All
Phase N/A

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Overview

Background
  • Cerebrospinal fluid (CSF) is the liquid around the brain and spinal cord. Many diseases can only be diagnosed by examining the CSF. A lumbar puncture is used to collect and test CSF. Once someone is already having a lumbar puncture, a small extra amount of CSF can be collected at the same time. This fluid can be used to study brain, nerve, and related health issues. Researchers want to collect CSF and blood samples from people who are scheduled to have a lumbar puncture.
    Objectives
  • To collect cerebrospinal fluid and blood samples from individuals who are having a lumbar puncture.
    Eligibility
  • Individuals between 2 and 100 years of age who are scheduled to have a lumbar puncture for clinical or research purposes.
    Design
  • Participants will have a lumbar puncture for clinical or research purposes.
  • During the procedure, an additional sample of CSF will be collected. They will also provide a blood sample, if one is not taken at the time of the procedure.
  • Treatment will not be provided as part of this study.

Description

In this study we are planning to establish a repository of cerebrospinal fluid (CSF), serum, and plasma. We are planning to collect a small amount of additional CSF and blood on subjects who are already going to have a lumbar puncture as part of their research or clinical care at the National Institutes of Health (NIH). This will allow us to study whether there is an association between neurological diseases and biomarkers, help identify novel pathogens infecting the central nervous system, and better enable us to understand the immune response to infections under future protocols. CSF and blood as well as clinical data associated with the samples will be stored securely.

Eligibility

  • SUBJECT INCLUSION CRITERIA:
    • Subjects (patients and healthy volunteers) 2 years of age and older identified to undergo LP for research or for clinical care purposes at the NIH Clinical Center.

SUBJECT EXCLUSION CRITERIA:

        -Subjects (patients and healthy volunteers) with the inability to provide informed consent
        either directly or via a legally authorized representative.
        Inclusion of Vulnerable Subjects - Research Involving Adults Who Are Or May Be Unable To
        Consent:
        -The risks to all subjects involved in this research project are no more than minimal risk
        as we are only collecting additional CSF and plasma during a LP procedure that is already
        being performed under a separate research protocol or as a clinically indicated procedure.
        At the time of the LP it will already be determined if the subject is able to give informed
        consent and if not a legally authorized representative will have been appointed who will
        decide if the additional CSF and plasma can be obtained from the individual.

Study details
    Nervous System Diseases

NCT01862107

National Institute of Neurological Disorders and Stroke (NINDS)

20 August 2025

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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