Phase II Randomized Study of Early Surgery Vs Multiple Sequential Antiepileptic Drug Therapy for Infantile Spasms Refractory to Standard Treatment
NCT ID: NCT00004758
Last Updated: 2005-06-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE2
30 participants
INTERVENTIONAL
1993-11-30
Brief Summary
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II. Assess how infantile spasms interfere with development and whether this is partially reversible.
III. Determine the predictors of good surgical outcome and whether surgery permanently controls seizures and improves development.
Detailed Description
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The second group undergoes surgical resection of the zone of cortical abnormality. A functional hemispherectomy is performed for hemiparesis or diffuse unihemispheric dysfunction.
If seizures are controlled in the first group at 3 months, the current medication is maintained; if seizures are not controlled, sequential therapy continues to completion. Patients experiencing uncontrolled seizures at 6 months cross to surgery.
Surgical patients experiencing uncontrolled seizures at 3 months or persistent seizures after taper of pre-study antiepileptics cross to drug therapy.
All patients are followed at 6 months and 1, 2, 3, 5, 7, and 10 years.
Conditions
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Study Design
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RANDOMIZED
TREATMENT
Interventions
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carbamazepine
corticotropin
nitrazepam
pyridoxine
valproic acid
Surgery
Eligibility Criteria
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Inclusion Criteria
Disease Characteristics
* Infantile spasms or seizures with diagnosis based on the following: short muscular contractions leading to flexion or extension; Single or repetitive electroencephalogram (EEG) consistent with diagnosis, i.e., hypsarrhythmia, modified hypsarrhythmia, multifocal spike and wave abnormalities; developmental quotient less than 70
* Zone of cortical abnormality in 1 lobe, contiguous multilobes, or 1 hemisphere; confirmed by historical, neurological, and physical evidence, including EEG, closed circuit televised EEG, computed tomography, magnetic resonance imaging, and/or positron-emission tomography; at least 2 abnormal test/imaging results required
* No treatable seizure etiology such as metabolic disease or infection
Prior/Concurrent Therapy
* Failed standard therapy, i.e., refractory to corticotropin (at least 40 IU/day for 14 days) as follows: persistent infantile spasms OR recurrent spasms after discontinuation or taper OR complications requiring dose modification
* At least 1 month of standard antiepileptic drug with documented therapeutic blood levels
Patient Characteristics
* No medical contraindication to surgery
* English-speaking family
0 Years
2 Years
ALL
No
Sponsors
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National Institute of Neurological Disorders and Stroke (NINDS)
NIH
University of California, Los Angeles
OTHER
National Center for Research Resources (NCRR)
NIH
Principal Investigators
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W. Donald Shields
Role: STUDY_CHAIR
University of California, Los Angeles
Other Identifiers
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UCLA-9508342
Identifier Type: -
Identifier Source: secondary_id
199/11691
Identifier Type: -
Identifier Source: org_study_id