ID
12026
Beschrijving
A Cross-Over, Multi-Center Trial to Evaluate the Diagnostic Efficacy and Safety of [123I]NAV5001 as an Imaging Agent to Aid in the Diagnosis of Parkinsonian Syndromes; ODM derived from: https://clinicaltrials.gov/show/NCT01950468 Principal Investigator: Stephen Flitman, M.D and Ira Goodman, M.D
Link
https://clinicaltrials.gov/show/NCT01950468
Trefwoorden
Versies (1)
- 01-09-15 01-09-15 -
Geüploaded op
1 september 2015
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Parkinson's Syndrome NCT01950468
Eligibility Parkinson's Syndrome NCT01950468
- StudyEvent: Eligibility
Beschrijving
Exclusion Criteria
Alias
- UMLS CUI-1
- C0680251
Beschrijving
Any clinically significant or unstable physical or psychological illness based on medical history or physical examination at screening, as determined by the investigator
Datatype
boolean
Alias
- UMLS CUI [1]
- C0205485
- UMLS CUI [2]
- C1658764
Beschrijving
Structural brain abnormality affecting the entire brain (e.g., normal pressure hydrocephalus) or the striatum (e.g., local tumor or stroke)
Datatype
boolean
Alias
- UMLS CUI [1]
- C0006111
Beschrijving
Any clinically significant abnormal laboratory results obtained at screening and as determined by the investigator
Datatype
boolean
Alias
- UMLS CUI [1]
- C1254595
- UMLS CUI [2]
- C0205161
Beschrijving
Any clinically significant abnormal electrocardiogram (ECG) results obtained at screening and as determined by the investigator
Datatype
boolean
Alias
- UMLS CUI [1]
- C2826714
- UMLS CUI [2]
- C0205161
Beschrijving
Any history of drug, narcotic, or alcohol abuse within 2 years before the date of informed consent, as defined by the Diagnostic and Statistical Manual of the American Psychiatric Association, Fourth Edition, revised (DSM-IV-TR [American Psychiatric Association, 1994])
Datatype
boolean
Alias
- UMLS CUI [1]
- C0013146
Beschrijving
Positive urine drug screen for opiates, cocaine, or amphetamines at screening
Datatype
boolean
Alias
- UMLS CUI [1]
- C0743300
Beschrijving
Positive pregnancy test before imaging
Datatype
boolean
Alias
- UMLS CUI [1]
- C0240802
Beschrijving
Participation in an investigational drug or device clinical trial within 30 days before the date of informed consent
Datatype
boolean
Alias
- UMLS CUI [1]
- C0679823
- UMLS CUI [2]
- C0008976
Beschrijving
Previous scan with any DAT imaging agent (e.g. [123I]NAV5001, Altropane, DaTscan, DOPASCAN)
Datatype
boolean
Alias
- UMLS CUI [1]
- C1512628
Beschrijving
Any exposure to radiopharmaceuticals within 30 days before the date of informed consent
Datatype
boolean
Alias
- UMLS CUI [1]
- C0182638
Beschrijving
Breast-feeding
Datatype
boolean
Alias
- UMLS CUI [1]
- C0006147
Beschrijving
Inability to lie supine for 1 hour
Datatype
boolean
Alias
- UMLS CUI [1]
- C0038846
Beschrijving
Any thyroid disease other than adequately treated hypothyroidism
Datatype
boolean
Alias
- UMLS CUI [1]
- C0040128
Beschrijving
Known sensitivity or allergy to iodine or iodine containing products
Datatype
boolean
Alias
- UMLS CUI [1]
- C0571818
- UMLS CUI [2]
- C0571817
Beschrijving
Treatment within the 30 days before the date of imaging with amoxapine, amphetamine, benztropine, bupropion, buspirone, cocaine, mazindol, methamphetamine, methylphenidate, norephedrine, phentermine, phenylpropanolamine, selegiline, and sertraline, paroxetine, or citalopram.
Datatype
boolean
Alias
- UMLS CUI [1]
- C1323365
- UMLS CUI [2]
- C1254351
Similar models
Eligibility Parkinson's Syndrome NCT01950468
- StudyEvent: Eligibility
C1658764 (UMLS CUI [2])
C0205161 (UMLS CUI [2])
C0205161 (UMLS CUI [2])
C0008976 (UMLS CUI [2])
C0571817 (UMLS CUI [2])
C1254351 (UMLS CUI [2])