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Completed

NCT Number: NCT01044758

Levetiracetam and Memory Function in Amnestic Mild Cognitive Impairment (MCI)

This research is being done to find out if daily use of the drug levetiracetam can improve memory function in individuals with memory problems like those associated with Mild Cognitive Impairment (MCI) and Alzheimer's disease (AD).

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Key information

About this study

Increasing research is focused on conditions that precede the clinical diagnosis of Alzheimer's disease (AD) in order to detect patients at risk for early intervention. One such condition is mild cognitive impairment (MCI). Functional magnetic resonance imaging (fMRI) studies in this group of patients have reported increased activation in the Medial Temporal Lobe (MTL) during performance of memory tasks. The functional significance of increased activation is unclear. One possibility is that greater activity reflects the increased effort needed in order to maintain performance, and as such would be a compensatory response. An alternative possibility is that increased activation reflects aberrant physiology related to the disease process itself and as such would be a sign of greater underlying disease severity and would interfere with brain function.

Data in animal models suggest the possibility that low dose levetiracetam (well-tolerated anti-convulsant) treatment may reduce the observed hyperactivity and improve memory performance among individuals with MCI. The investigators are therefore conducting a within-subjects trial of 8 weeks duration, involving 144 subjects and low dose treatment with levetiracetam. During the course of the study, each subject may receive both drug and placebo for two weeks, with the order of administering those treatments counterbalanced. Cognitive testing and fMRI imaging will be obtained after 2-weeks on drug/placebo. The overall goal of the study is to determine if treatment of MCI subjects with low dose levetiracetam reduces hyperactivity within the MTL and improves memory performance.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All: English as a first language; right handed; able to complete written informed consent.
  • MCI subjects: In addition to above, must meet criteria for amnestic Mild Cognitive Impairment (MCI). This includes a memory complaint corroborated by an informant; impaired memory function for age and educational level; preserved general cognitive function; intact abilities of daily living; no clinical dementia.
  • Age matched Controls: Must have memory and cognitive status that is normal for their age.

Exclusion criteria

  • Familial Alzheimer's Disease (AD) due to known genetic mutations
  • AD with Parkinsonian features; major psychiatric or behavioral disorders (e.g. depression, agitation, psychosis, manic-depressive disorder)
  • Primary or metastatic intracranial neoplasm
  • History of severe head trauma
  • Intra-cerebral hemorrhage
  • Seizure disorder
  • Hemispheric stroke
  • Presence of a progressive central nervous system disease
  • Presence of lacunar infarcts
  • Medical contraindications to MRI including cardiac pacemaker, presence of intraocular or intracranial metallic objects
  • Any known allergy to levetiracetam or behavioral problems that are a contraindication to taking Levetiracetam (e.g. agitation)
  • Prescribed use of anti-seizure medications.

Treatment and study plan

Levetiracetam 62.5mg

Drug

62.5mg twice daily (2 weeks)

Other names: Keppra

Levetiracetam 125mg

Drug

125mg twice daily (2 weeks)

Other names: Keppra

Levetiracetam 250mg

Drug

250mg twice daily (2 weeks)

Other names: Keppra

Placebo

Drug

placebo capsule twice daily (2 weeks)

Primary outcomes

  1. Brain Activity in the Dentate Gyrus / CA3 Subregion of the Hippocampus Measured With Blood Oxygenation Level Dependent (BOLD) Functional MRI

    Time frame: 2 weeks

    Measurement of average brain activity in the dentate gyrus / CA3 subregion of the hippocampus measured with BOLD functional MRI in patients with mild cognitive impairment on placebo and on drug compared to average brain activity in this brain area in control subjects.

Secondary outcomes

  1. Behavioral Performance as Assessed in the Functional Magnetic Resonance Imaging (fMRI) Memory Task

    Time frame: 2 weeks

    Mnemonic similarity task which assesses long term memory function. Scale ranges from 0-100 with higher scores indicating better memory performance.

Sponsors and collaborators

Lead sponsor

Johns Hopkins University

Other

Collaborators

  • National Institute on Aging (NIA)

Registry information

Official study title

Bridging Cognitive Aging in Rodents to Man Using fMRI in Amnestic MCI

Important dates

Study start
2009
Primary completion
2012
Study completion
2012
First posted
Jan 8, 2010
Registry last updated
Aug 21, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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