IV Keppra in the Emergency Department for Prevention of Early Recurrent Seizures
Information source: Emory University
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Tonic-clonic Seizure
Intervention: Keppra (Drug); Fosphenytoin (Drug); Dilantin (Drug)
Phase: Phase 4
Status: Completed
Sponsored by: Emory University Official(s) and/or principal investigator(s): Debra Houry, MD, Principal Investigator, Affiliation: Emory University
Summary
This study is looking at three seizure medicines. Patients with seizures are usually
treated with phenytoin (Dilantin) or Fosphenytoin. These medicines can be given
intravenously (IV)or by mouth. Another seizure medicine, levetiracetam (Keppra) can now be
given this way also. This study will compare IV phenytoin (Dilantin) and IV fosphenytoin to
levetiracetam (Keppra) in patients who have had a recent seizure. Only patients with a
history of seizures can be involved. The patient must present to the emergency department
within 4 hours of a seizure. The purpose of this study is to compare these three drugs,
phenytoin (Dilantin), fosphenytoin, and levetiracetam (Keppra). The investigators are
looking to see if these drugs can prevent another seizure in the next 24 hours. We are also
looking for any possible side effects.
Clinical Details
Official title: IV Keppra in the Emergency Department for Prevention of Early Recurrent Seizures
Study design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Primary outcome: Number of Participants Who Experienced a Recurrent Seizure After Treatment.
Detailed description:
More than one in every one hundred patients presenting to the emergency department for care
do so for seizures. More than half of these patients will require medications, often
intravenously (IV), while in the emergency department. For many years the standard
treatment has been phenytoin. However, there are many known contraindications to the use of
this drug. These include known hypersensitivity, cardiac arrhythmias, cardiac disease,
impaired liver or kidney function, diabetes mellitus, older age, thyroid disease, pregnancy,
and alcohol use. A recent review of patients with seizure disorder at Emory Crawford Long
and Emory University hospitals suggested that a significant percentage of those who were
taking phenytoin actually had one or more of these contraindications. Additionally, the IV
form of phenytoin has known, severe adverse effects including cardiovascular collapse, life
threatening cardiac arrhythmias, and severe hypotension. There is another form of
Phenytoin, called Fosphenytoin, that while safer in some respects still has similar concerns
associated with its administration.
Levetiracetam (Keppra) has been available as an oral drug in the United States since 2000
and has a well established safety record when used as an add-on drug for patients with
partial onset seizures. A double-blinded randomized study has shown that levetiracetam is
also effective for primary generalized seizures as well.
The IV form of levetiracetam has recently been approved by the FDA for use. The only known
contraindications other than known hypersensitivity include impaired renal function,
psychiatric disorder, older age, and pregnancy. IV levetiracetam is not known to cause any
of the acute, catastrophic events seen occasionally with phenytoin.
The investigators would therefore like to compare IV phenytoin and fosphenytoin to IV
levetiracetam in preventing early recurrent seizures. Patients with known seizure disorders
would be randomly assigned to one of two groups and therefore receive either IV fosphenytoin
or IV levetiracetam. After an observation period, seizure free patients would be discharged
and 24 hour phone follow up conducted to assess for the effectiveness of these anti-seizure
medications as well as for any adverse reactions.
Eligibility
Minimum age: 18 Years.
Maximum age: N/A.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- age 18 or older
- patient presenting to Grady Memorial Hospital's Emergency Department after having a
tonic-clonic seizure (primary or secondarily generalized) within the last 4 hours
Cause of seizure for inclusion: reason for seizure is often undetermined at time of
presentation to the Emergency Department. The most likely expected causes of a seizure
are noncompliance to existing antiepileptic drug regimen, refractory epilepsy with
breakthrough seizure, metabolic aberration, alcohol withdrawal, or unknown.
Exclusion Criteria:
- non-English speaking
- first time seizure
- seizures other than tonic-clonic seizure (primary or secondarily generalized)
- more than 3 seizures in 24 hours or status epilepticus, pregnant patients by history
or by urine pregnancy testing, serious neurologic insult resulting in seizure but
where seizure is not the primary reason for admission (e. g. traumatic brain injury
with seizure or hemorrhagic stoke would be excluded)
- contraindication to IV levetiracetam
- received IV phenytoin within 24 hours
- known allergy to phenytoin
- previously enrolled in the study
Locations and Contacts
Grady Memorial Hospital, Atlanta, Georgia 30303, United States
Additional Information
Starting date: July 2007
Last updated: November 18, 2013
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