WBC: Establishment of a Tissue Bank (Blood, CSF) for the Understanding of Motor Neuron Disease (MND)

Sponsor
Wake Forest University Health Sciences (Other)
Overall Status
Terminated
CT.gov ID
NCT01950910
Collaborator
(none)
766
1
199
3.8

Study Details

Study Description

Brief Summary

Biomarkers are essential for the identification of disease states. There are no early diagnostic or prognostic markers for ALS. The purpose of this study is to identify a panel of biomarkers from blood or spinal fluid of ALS patients and to collect data to better understand disease progression.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Amyotrophic lateral sclerosis (ALS) is a motor neuron disease characterized by progressive degeneration of motor neurons, muscle atrophy and paralysis. There is no reliable early diagnostic test for ALS making identification of the disease difficult at its earliest stages. Early detection is critical to the initiation of early neuroprotective therapy. By the time a reliable diagnosis can be made, substantial damage to motor neurons and muscle has already occurred. The purpose of the current project is to establish a bank of blood samples (serum and protein/RNA/DNA from blood cells) and CSF for use in the development of an early diagnostic test for ALS and to better understand the progression of this disease.

    Samples from patients that have a confirmed or unknown diagnosis of motor neuron disease will be examined. ALS and suspected neuromuscular disease (control) samples will be collected for comparison. Investigators will examine various biochemical, metabolic and genetic markers from these samples in hopes of finding differences in the expression between control subjects and ALS patients and how these biomarkers vary during disease progression. Participants will be asked to complete an optional questionnaire to collect data including medication and vitamin use and medical and disease history. This data will be linked to the patient's samples; however, all samples will be deidentified and coded to avoid the possibility of linking results to the patient. Results will not be stored in the patient's medical record.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    766 participants
    Observational Model:
    Other
    Time Perspective:
    Prospective
    Official Title:
    Establishment of a Tissue Bank (Blood, CSF) for the Understanding of the Disease Progression and Early Diagnosis of Motor Neuron Disease (MND).
    Actual Study Start Date :
    Mar 29, 2004
    Actual Primary Completion Date :
    Dec 31, 2017
    Actual Study Completion Date :
    Oct 29, 2020

    Arms and Interventions

    Arm Intervention/Treatment
    subjects w/ non-motor neurodegenerative disease

    subjects with ALS or with non-motor neurodegenerative disease

    subjects w/out motorneuron degenerative dis

    subjects without motorneuron degenerative disease

    Outcome Measures

    Primary Outcome Measures

    1. Levels of ALS biomarkers in blood [After blood is collected from study subjects. Data will be analyzed at one year.]

      Blood samples will be processed to obtain serum samples and to isolate peripheral blood mononuclear cells (PBMC's). Serum samples will be analyzed for biochemical and metabolic markers of interest and future cell culture as needed. PBMCs will be processed for RNA, DNA or protein isolation. Aliquots of all samples will be stored for future study.

    2. Levels of ALS biomarkers in CSF [After CSF is collected from study subject. Data will be analyzed at one year.]

      CSF samples will be processed and assayed for biomarkers of interest. An aliquot of CSF sample will be stored for future study.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • 18 years old or older
    Exclusion Criteria:
    • less than 18 years old

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Neurosciences Institute, Neurology - Charlotte Charlotte North Carolina United States 28207

    Sponsors and Collaborators

    • Wake Forest University Health Sciences

    Investigators

    • Principal Investigator: Benjamin R Brooks, MD, Neurosciences Institute, Neurology - Charlotte

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Wake Forest University Health Sciences
    ClinicalTrials.gov Identifier:
    NCT01950910
    Other Study ID Numbers:
    • CHS-Neurology-WBC Tissue Bank
    First Posted:
    Sep 26, 2013
    Last Update Posted:
    Jul 11, 2022
    Last Verified:
    Jul 1, 2022
    Keywords provided by Wake Forest University Health Sciences
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 11, 2022