Single Photon Emission Computed Tomography (SPECT) to Study Paroxysmal Hyperkinetic Movement Disorders
The Physiology of Paroxysmal Hyperkinetic Movement Disorders: A SPECT Study
2 other identifiers
observational
40
1 country
1
Brief Summary
This study will use single photon emission computed tomography (SPECT) to determine what areas of the brain are responsible for paroxysmal hyperkinetic movement disorders. Patients with these disorders have sudden, brief attacks of movement, similar to epileptic seizures, but without loss of consciousness. SPECT is a nuclear medicine test that produces three-dimensional images of the brain, showing blood flow and function in different brain regions. This test, which can detect the focus of epileptic seizures, will be used in this study to scan patients while they are experiencing a hyperkinetic movement attack, while they are not having and attack, and while they are simulating an attack. Patients 18 years of age and older who have paroxysmal movement attacks that can be easily induced by a specific trigger, such as a sudden movement or prolonged exercise, may be eligible for this study. Candidates will be screened with a medical history and review of their medical records, physical examination, videotape of attacks, and, for women, a pregnancy test. Participants will have three SPECT scans, separated from each other by at least 48 hours. Before each scan, the subject will perform an activity that ordinarily precipitates a movement attack, such as standing up from a chair, assuming a certain posture, or doing something strenuous. Each scan will try to record one of the following conditions:
- The subject performs the trigger activity, but does not have an attack;
- The subject performs the trigger activity and has an involuntary attack as a result;
- The subject performs the trigger activity and does not have an attack, but then mimics an attack voluntarily. After the condition is recorded, the subject will be given an injection of a radioactive agent called 99m Technetium and will then relax quietly for 40 to 60 minutes before the SPECT scan. For the scan, the subject lies on an examination table and the SPECT camera is moved near and around the head to image the brain. The scan takes about 40 minutes. Participants will also undergo one magnetic resonance imaging (MRI) scan. For this test, the subject lies in a narrow cylinder (the scanner), while pictures of the brain are taken. Earplugs are worn to muffle loud noises caused by electrical switching of radio frequency circuits used in the scanning process. The procedure takes about 30 minutes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Jan 2003
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2003
CompletedFirst Submitted
Initial submission to the registry
January 8, 2003
CompletedFirst Posted
Study publicly available on registry
January 9, 2003
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2005
CompletedMarch 4, 2008
January 1, 2005
January 8, 2003
March 3, 2008
Conditions
Keywords
Eligibility Criteria
You may qualify if:
- Established diagnosis of paroxysmal hyperkinetic movement disorders. The diagnosis will be established by the preliminary screening in the NINDS Movement Disorders Outpatient Clinic, based on review of medical record, history, clinical evaluation, and video tapes of an attack.
- Age 18 or older.
- A reproducible trigger of paroxysmal hyperkinetic attacks, such as sudden movement, or prolonged exercise, which will produce attacks at least with 50% consistency.
- Patients only with paroxysmal attacks of hyperkinetic movements.
- Patients whose attacks can be precipitated easily.
- Patients whose typical attack last at least 15 seconds.
- Patients taking medication that may influence the central nervous system, such as phenytoin, phenobarbital, carbamazepine, clonazepam, and antidepressants (but not limited to these) for their paroxysmal dyskinesias (not seizures) will be asked to hold the medication prior to the study. A sufficient drug washout period will be established dependant upon the individual drug. Subjects may be admitted to the NIH if necessary. They will be asked to abstain from alcohol and caffeine 24 hours prior to the study as well.
- Established diagnosis of psychogenic hyperkinetic movement disorders. The diagnosis will be established by the preliminary screening in the NINDS Movement Disorders Outpatient Clinic, based on review of medical record, history, clinical evaluation, and video tapes of an attack.
- Patients with clear onset, stereotyped, defined and evaluable hyperkinetic attacks.
- Patients only with paroxysmal attacks of hyperkinetic movements.
- Age 18 or older.
- A reproducible trigger of paroxysmal hyperkinetic attacks, such as sudden movement, startle or prolonged exercise, which will produce attacks at least with 50% consistency.
- Patients whose attacks can be precipitated easily.
- Patients whose typical attack last at least 15 seconds.
- Patients taking medication that may influence the central nervous system, such as phenytoin, phenobarbital, carbamazepine, clonazepam, and antidepressants (but not limited to these) will be asked to hold the medication prior to the study. A sufficient drug washout period will be established dependant upon the individual drug. Subjects may be admitted to the NIH if necessary. They will be asked to abstain from alcohol and caffeine 24 hours prior to the study as well.
You may not qualify if:
- Age younger than 18 years old.
- Previous history of or MRI findings consistent with brain tumors, strokes, trauma or arterial venous malformations.
- Contraindication to MRI such as having devices not compatible with MRI (pacemaker, an implanted medical pump, brain stimulators etc.), metallic prostheses in their body (metal pins and rods, heart valves, cochlear implants etc.), and history of working with metals in the past, since such persons may potentially have small metal fragments in the eye without being aware of it.
- Any diagnosis of progressive neurological disorders other than paroxysmal hyperkinetic movement disorder.
- Any history of significant medical disorders requiring chronic treatment with other drugs that affect the CNS, which cannot be stopped.
- Ongoing radiation therapy for medical condition such as cancer.
- Women who are pregnant or nursing. Female subjects of child bearing potential will have specific interview and a pregnancy test prior to the study (before each imaging procedure if required) to ensure that they are not pregnant or nursing.
- Any subject who is not capable of giving an informed consent. This will be determined at the initial evaluation at NINDS clinic. Patients with Mini Mental Score less than 25 or significant psychiatric history will be further evaluated by detailed neuropsychiatric testing, or consultation with a psychiatrist.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
National Institute of Neurological Disorders and Stroke (NINDS)
Bethesda, Maryland, 20892, United States
Related Publications (3)
Demirkiran M, Jankovic J. Paroxysmal dyskinesias: clinical features and classification. Ann Neurol. 1995 Oct;38(4):571-9. doi: 10.1002/ana.410380405.
PMID: 7574453BACKGROUNDKertesz A. Paroxysmal kinesigenic choreoathetosis. An entity within the paroxysmal choreoathetosis syndrome. Description of 10 cases, including 1 autopsied. Neurology. 1967 Jul;17(7):680-90. doi: 10.1212/wnl.17.7.680. No abstract available.
PMID: 6067487BACKGROUNDStevens H. Paroxysmal choreo-athetosis. A form of reflex epilepsy. Arch Neurol. 1966 Apr;14(4):415-20. doi: 10.1001/archneur.1966.00470100071009. No abstract available.
PMID: 5906466BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Sponsor Type
- NIH
Study Record Dates
First Submitted
January 8, 2003
First Posted
January 9, 2003
Study Start
January 1, 2003
Study Completion
January 1, 2005
Last Updated
March 4, 2008
Record last verified: 2005-01