Relationship of HHV-6B Virus to Seizures and Brain Injury

Sponsor
National Institute of Neurological Disorders and Stroke (NINDS) (NIH)
Overall Status
Terminated
CT.gov ID
NCT00597285
Collaborator
(none)
33
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Study Details

Study Description

Brief Summary

This study will look for evidence that a virus called HHV-6B may be related to seizures and to a form of brain injury called mesial temporal sclerosis that is associated with seizures. The study will use new, more sensitive brain scans to try to detect brain regions that might be affected by the virus and will examine cerebrospinal fluid (CSF, the fluid that bathes the brain and spinal cord) for evidence of the virus as well.

Healthy volunteers and people with seizures uncontrolled by anti-epileptic drugs who are between 18 and 45 years of age may be eligible for this study. Candidates are screened with a physical examination and laboratory tests.

Participants undergo the following procedures:
  • PET scan. This test uses a radioactive chemical called 18FDG, which is detected by the PET scanner to obtain images of the brain. The subject lies on a table with his or her head positioned in the scanner. A swimming cap with a small light reflector is placed on the head to monitor the position of the head during the scan. A catheter (plastic tube) is inserted into an artery at the wrist or elbow crease of the arm for obtaining blood samples during the scan, and a second catheter is placed in a vein in the other arm for injecting the 18FDG. The scan takes up to 2 hours. A second scan may be done over an additional 15 minutes.

  • MRI. This test uses a strong magnetic field and radio waves to obtain images of the brain. The subject lies on a table that can slide in and out of a metal cylinder surrounded by a magnetic field. Most scans last between 45 and 90 minutes.

  • Lumbar puncture. The subject sits upright or lies on a table with the knees curled to the chest for this procedure. A local anesthetic is injected to numb the skin and a needle is inserted in the space between the bones in the lower back where the CSF circulates below the spinal cord. A small amount of fluid is collected through the needle.

  • Blood tests. About 4 tablespoons of blood are drawn for viral tests.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Objectives: 1) to attempt to detect specific patterns of hippocampal injury in patients with temporal lobe epilepsy that may be associated with HHV-6B infection; 2) To attempt to detect evidence for persistent HHV6 infection in CSF in patients with refractory temporal lobe epilepsy. 3) to obtain preliminary pilot data on the ability of high resolution structural to detect abnormalities in epilepsy patients not seen with standard scanners.

    Study Population: 45 patients with localization-related epilepsy; 45 healthy volunteers

    Design: 1) imaging with a 7T MRI magnetic resonance scanner; 2) Lumbar puncture. 3) blood sampling

    Main outcome measure: 1) Detection of evidence for HHV6 infection in CSF

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    33 participants
    Time Perspective:
    Prospective
    Official Title:
    HHV6B in Epilepsy Imaging and CSF Studies
    Study Start Date :
    Jan 3, 2008
    Study Completion Date :
    Nov 1, 2013

    Outcome Measures

    Primary Outcome Measures

    1. Detection of evidence for HHV6 infection in CSF []

    Secondary Outcome Measures

    1. Detection of lesions on 7T compared to 3T MRI []

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 55 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    • INCLUSION CRITERIA:

    Patients will be avaluated for participation under screening protocol 01-N-0139.

    Patients

    Male and female subjects age 18 to 55

    Subjects with seizures uncontrolled by antiepileptic drugs

    Subjects with no other illnesses, or taking other substances or medicines that could interfere with the study

    Healthy Controls

    Male and female subjects age 18 to 55.

    EXCLUSION CRITERIA:

    Patient

    Subjects who are pregnant or breast feeding.

    Subjects with any medical condition that could interfere with the study.

    Subjects who are taking drugs that significantly reduce blood clotting such as Coumadin or Warfarin.

    Healthy Volunteers

    Subjects who are pregnant or breast feeding

    Subjects who have any medical condition or be taking any substance or medication that could interfere with the study

    Subjects who are taking drugs that significantly reduce blood cloting such as Coumadin or Warfarin

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda Maryland United States 20892

    Sponsors and Collaborators

    • National Institute of Neurological Disorders and Stroke (NINDS)

    Investigators

    • Principal Investigator: William H Theodore, M.D., National Institute of Neurological Disorders and Stroke (NINDS)

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00597285
    Other Study ID Numbers:
    • 080027
    • 08-N-0027
    First Posted:
    Jan 18, 2008
    Last Update Posted:
    Dec 16, 2019
    Last Verified:
    Nov 1, 2013
    Keywords provided by , ,
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Dec 16, 2019