Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 5:36 PM
Ignite Modification Date:
2025-12-24 @ 5:36 PM
NCT ID:
NCT01950468
Eligibility Criteria:
Inclusion Criteria:
* Subject has provided written informed consent before the initiation of any study related procedures and continues to give willing consent for participation
* Age ≥ 40 years
* Have had upper extremity tremor for \< 3 years duration, regardless of presumed diagnosis or etiology
* Have a UPDRS part III score upon entry of ≤ 16
Exclusion Criteria:
* Any clinically significant or unstable physical or psychological illness based on medical history or physical examination at screening, as determined by the investigator
* Structural brain abnormality affecting the entire brain (e.g., normal pressure hydrocephalus) or the striatum (e.g., local tumor or stroke)
* Any clinically significant abnormal laboratory results obtained at screening and as determined by the investigator
* Any clinically significant abnormal electrocardiogram (ECG) results obtained at screening and as determined by the investigator
* 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 \[American Psychiatric Association, 1994\])
* Positive urine drug screen for opiates, cocaine, or amphetamines at screening
* Positive pregnancy test before imaging
* Participation in an investigational drug or device clinical trial within 30 days before the date of informed consent
* Previous scan with any DAT imaging agent (e.g. \[123I\]NAV5001, Altropane, DaTscan, DOPASCAN)
* Any exposure to radiopharmaceuticals within 30 days before the date of informed consent
* Breast-feeding
* Inability to lie supine for 1 hour
* Any thyroid disease other than adequately treated hypothyroidism
* Known sensitivity or allergy to iodine or iodine containing products
* 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.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
40 Years
Study:
NCT01950468
Study Brief:
Protocol Section:
NCT01950468