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Antiepileptic Drugs and Vascular Risk Markers

Primary Purpose

Subarachnoid Hemorrhage

Status
Terminated
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
phenytoin
valproate
levetiracetam
Sponsored by
Thomas Jefferson University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Subarachnoid Hemorrhage focused on measuring vascular risk, lipid fractions, lipoprotein(a), C-reactive protein, subarachnoid hemorrhage, antiepileptic drug, randomized, seizure, cholesterol

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Acute subarachnoid hemorrhage, Hunt-Hess Grades I-IV
  • Within 48 hours of admission

Exclusion Criteria:

  • Grade V subarachnoid hemorrhage
  • Being treated with a lipid-lowering agent
  • Contraindication to phenytoin, valproate, or levetiracetam (e.g. history of allergy to one of these agents)
  • Contraindication to receiving no antiepileptic drug treatment (e.g. history of pre-existing epilepsy, seizure activity on admission EEG)

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm 4

    Arm Type

    Active Comparator

    Active Comparator

    Active Comparator

    No Intervention

    Arm Label

    1

    2

    3

    4

    Arm Description

    Participants randomized to Group 1 will receive phenytoin (PHT) at 5 mg/kg/day in 2 divided doses.

    Participants randomized to Group 2 will receive valproate (VPA) at 15 mg/kg/day in 3 divided doses or in a once-daily extended release formulation.

    Participants randomized to Group 3 will receive levetiracetam (LEV) 1000-1500 mg/day in 2 divided doses.

    Participants randomized to Group 4 will receive no drug intervention.

    Outcomes

    Primary Outcome Measures

    Change in Serum Cholesterol, Non-HDL Cholesterol, HDL Cholesterol, Lipoprotein(a), and C-reactive Protein From Baseline to Second Draw and Third Draw in Each of the 4 Study Arms

    Secondary Outcome Measures

    Incidence of Acute Seizures, Incidence of Late Seizures, Overall Neurologic Function (as Measured by Modified Rankin Scale Scores)

    Full Information

    First Posted
    October 16, 2008
    Last Updated
    December 14, 2017
    Sponsor
    Thomas Jefferson University
    Collaborators
    National Institute of Neurological Disorders and Stroke (NINDS)
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00774306
    Brief Title
    Antiepileptic Drugs and Vascular Risk Markers
    Official Title
    The Effects of Antiepileptic Drugs on Serum Lipids and Inflammation in Patients With Subarachnoid Hemorrhage
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    December 2017
    Overall Recruitment Status
    Terminated
    Why Stopped
    study no longer consistent with current clinical practice
    Study Start Date
    April 2009 (undefined)
    Primary Completion Date
    June 2012 (Actual)
    Study Completion Date
    June 2012 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Thomas Jefferson University
    Collaborators
    National Institute of Neurological Disorders and Stroke (NINDS)

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The purpose of this study is to determine if certain seizure medications raise levels of cholesterol and other blood components which could increase the risk of heart attacks and strokes.
    Detailed Description
    There is some evidence that certain seizure medicines may raise levels of cholesterol and other blood components which could increase the risk of heart attacks and strokes, however, more research is needed. Individuals with acute subarachnoid hemorrhage traditionally are treated with seizure medicines, but it is not clear which one is best, or if any such medication is necessary at all. This study is intended to find out if certain seizure medications raise levels of cholesterol and other blood components which could lead to an increased risk of heart attacks and strokes. In this study, 200 people with acute subarachnoid hemorrhage will be randomized to treatment with one of three different seizure medicines-phenytoin, valproate, or levetiracetam-or to receive no seizure medication at all. In each participant, cholesterol and other blood markers that relate to heart attack and stroke risk will be measured shortly after hospital admission and again 8 weeks later. At the 8-week point most participants will have their seizure medication discontinued, and the same blood tests will be repeated. Information from this study could lead to changes in how seizure medications are prescribed both in the subarachnoid hemorrhage population and in other people who are prone to seizures.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Subarachnoid Hemorrhage
    Keywords
    vascular risk, lipid fractions, lipoprotein(a), C-reactive protein, subarachnoid hemorrhage, antiepileptic drug, randomized, seizure, cholesterol

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    52 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    1
    Arm Type
    Active Comparator
    Arm Description
    Participants randomized to Group 1 will receive phenytoin (PHT) at 5 mg/kg/day in 2 divided doses.
    Arm Title
    2
    Arm Type
    Active Comparator
    Arm Description
    Participants randomized to Group 2 will receive valproate (VPA) at 15 mg/kg/day in 3 divided doses or in a once-daily extended release formulation.
    Arm Title
    3
    Arm Type
    Active Comparator
    Arm Description
    Participants randomized to Group 3 will receive levetiracetam (LEV) 1000-1500 mg/day in 2 divided doses.
    Arm Title
    4
    Arm Type
    No Intervention
    Arm Description
    Participants randomized to Group 4 will receive no drug intervention.
    Intervention Type
    Drug
    Intervention Name(s)
    phenytoin
    Other Intervention Name(s)
    Dilantin, Cerebyx (a phenytoin pro-drug)
    Intervention Description
    Phenytoin is a anti-seizure medication. Participants will receive phenytoin (PHT) at 5 mg/kg/day in 2 divided doses.
    Intervention Type
    Drug
    Intervention Name(s)
    valproate
    Other Intervention Name(s)
    Depakote, Depacon
    Intervention Description
    Valproate is an anti-seizure medication. Participants will receive valproate (VPA) at 15 mg/kg/day in 3 divided doses.
    Intervention Type
    Drug
    Intervention Name(s)
    levetiracetam
    Other Intervention Name(s)
    Keppra
    Intervention Description
    Levetiracetam is an anti-seizure medication. Participants will receive levetiracetam (LEV) 1000-1500 mg/day in 2 divided doses.
    Primary Outcome Measure Information:
    Title
    Change in Serum Cholesterol, Non-HDL Cholesterol, HDL Cholesterol, Lipoprotein(a), and C-reactive Protein From Baseline to Second Draw and Third Draw in Each of the 4 Study Arms
    Time Frame
    8 weeks, 16 weeks
    Secondary Outcome Measure Information:
    Title
    Incidence of Acute Seizures, Incidence of Late Seizures, Overall Neurologic Function (as Measured by Modified Rankin Scale Scores)
    Time Frame
    8 weeks, 16 weeks

    10. Eligibility

    Sex
    All
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Acute subarachnoid hemorrhage, Hunt-Hess Grades I-IV Within 48 hours of admission Exclusion Criteria: Grade V subarachnoid hemorrhage Being treated with a lipid-lowering agent Contraindication to phenytoin, valproate, or levetiracetam (e.g. history of allergy to one of these agents) Contraindication to receiving no antiepileptic drug treatment (e.g. history of pre-existing epilepsy, seizure activity on admission EEG)
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Scott Mintzer, MD
    Organizational Affiliation
    Assistant Professor of Neurology, Jefferson Comprehensive Epilepsy Center
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    Antiepileptic Drugs and Vascular Risk Markers

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