Study of Individuals With Parkinson's Symptoms But in Whom There is Diagnostic Uncertainty
Primary Purpose
Parkinsonian Syndrome
Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
[123I]ß CIT
Sponsored by
About this trial
This is an interventional diagnostic trial for Parkinsonian Syndrome focused on measuring parkinson, diagnosis
Eligibility Criteria
Inclusion Criteria: Age >21 Any parkinsonian or extrapyramidal symptoms Parkinsonian symptoms for < 2 years duration. No significant abnormalities on screening laboratory studies including: CBC, Chem-20 and urinalysis. Willingness to comply with study protocol. Exclusion Criteria: Pregnancy Significant medical disease including abnormalities on screening biochemical or hematological labs or abnormal electrocardiogram (ECG).
Sites / Locations
- Institute for Neurodegenerative Disorders
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
[123I]ß CIT
Arm Description
To assess [123I]ß CIT and SPECT imaging
Outcomes
Primary Outcome Measures
Comparison of the imaging diagnosis, based on visual analysis and quantitative analysis, to the clinical diagnosis of the investigator blinded to the imaging results
Secondary Outcome Measures
Comparison of the DAT imaging diagnosis, initial diagnosis by the movement disorder experts and referral neurologist diagnosis to the 'gold standard' diagnosis
Full Information
NCT ID
NCT00129675
First Posted
August 11, 2005
Last Updated
July 14, 2014
Sponsor
Institute for Neurodegenerative Disorders
Collaborators
Molecular NeuroImaging
1. Study Identification
Unique Protocol Identification Number
NCT00129675
Brief Title
Study of Individuals With Parkinson's Symptoms But in Whom There is Diagnostic Uncertainty
Official Title
Development of a Imaging Marker for Parkinson's Disease Through Use of Dynamic SPECT Imaging With [123I] Beta-CIT in Individuals With Parkinson's Symptoms
Study Type
Interventional
2. Study Status
Record Verification Date
July 2014
Overall Recruitment Status
Completed
Study Start Date
February 2003 (undefined)
Primary Completion Date
May 2009 (Actual)
Study Completion Date
May 2009 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Institute for Neurodegenerative Disorders
Collaborators
Molecular NeuroImaging
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The overall goal of this study is to evaluate the use of dopamine transporter (DAT) imaging as a diagnostic tool in subjects with early parkinsonian symptoms, in whom Parkinson's disease (PD) or parkinsonian syndrome (PS) is suspected, but the diagnosis remains unclear from a clinical standpoint.
Detailed Description
Subjects will be referred to the Institute for Neurodegenerative Disorders (IND) by practicing general neurologists with genuine uncertainty regarding the subject's diagnosis.
Subjects with suspected PD or PS will be evaluated clinically and with DAT imaging, using b-CIT and SPECT. The DAT imaging procedure will take place over two days:
On the first day participants are injected with [123I]ß CIT, an investigational radioactive material that localizes in the brain. Study participants will also have a thorough neurologic examination and standard neuropsychological testing, including testing of memory, concentration, abstraction and visual spatial functions.
Twenty-four hours later study participants return to the Institute for Neurodegenerative Disorders where an investigational scanning procedure will be used to obtain SPECT (single photon emission computed tomography) images of the brain.
Subjects will be asked to return within 3 months following the imaging study to have a repeat neurological examination by the two study neurologists at IND.
Subjects will be asked to return at about 6 months and possibly again at one year following the imaging study for a final clinical evaluation by one of the study neurologists at IND.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parkinsonian Syndrome
Keywords
parkinson, diagnosis
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
Participant
Allocation
N/A
Enrollment
169 (Actual)
8. Arms, Groups, and Interventions
Arm Title
[123I]ß CIT
Arm Type
Experimental
Arm Description
To assess [123I]ß CIT and SPECT imaging
Intervention Type
Drug
Intervention Name(s)
[123I]ß CIT
Other Intervention Name(s)
SPECT imaging
Intervention Description
Single Photon Emission Computed Tomography
SPECT imaging uses the single photon emissions from radioactive compounds that are (most commonly) injected into a patient and are metabolized by specific organs or body systems. SPECT imaging is performed by using a gamma camera to acquire multiple 2-D images (also called projections), from multiple angles. A computer is then used to apply a tomographic reconstruction algorithm to the multiple projections, yielding a 3-D dataset. This dataset may then be manipulated to show thin slices along any chosen axis of the body, similar to those obtained from other tomographic techniques, such as MRI, CT, and PET. The resulting SPECT images reflect body/organ function as opposed to specific anatomy of other imaging modalities such as CT or MRI.
Primary Outcome Measure Information:
Title
Comparison of the imaging diagnosis, based on visual analysis and quantitative analysis, to the clinical diagnosis of the investigator blinded to the imaging results
Time Frame
5 years
Secondary Outcome Measure Information:
Title
Comparison of the DAT imaging diagnosis, initial diagnosis by the movement disorder experts and referral neurologist diagnosis to the 'gold standard' diagnosis
Time Frame
5 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age >21
Any parkinsonian or extrapyramidal symptoms
Parkinsonian symptoms for < 2 years duration.
No significant abnormalities on screening laboratory studies including: CBC, Chem-20 and urinalysis.
Willingness to comply with study protocol.
Exclusion Criteria:
Pregnancy
Significant medical disease including abnormalities on screening biochemical or hematological labs or abnormal electrocardiogram (ECG).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Danna L Jennings, MD
Organizational Affiliation
Institute for Neurodegenerative Disorders
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institute for Neurodegenerative Disorders
City
New Haven
State/Province
Connecticut
ZIP/Postal Code
06510
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Study of Individuals With Parkinson's Symptoms But in Whom There is Diagnostic Uncertainty
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