Dementia With Lewy Bodies Clinical Trial
— IBVM/DATSCANOfficial title:
In Vivo SPECT Imaging of Vesicular Acetylcholine and Dopamine Transporters in Dementia With Lewy Bodies: Applying in Diagnostic and Identification of Pathological Subtypes.
The general aim of this research project is to determine the relationships between
alterations of central cholinergic (ACh) and dopaminergic (DA) systems and neurobehavioral
features of dementias with Lewy bodies (DLB).
Both clinical and neurochemical data support the view that DLB is not a homogeneous entity
and it can be hypothesized that differential alterations of central ACh systems (i.e.
anterior vs posterior vs striatal interneurons) in association or not with a DA
nigrostriatal dysfunction could partly support the clinical heterogeneity observed in this
disease. ACh in vivo imaging has been relatively underutilized to date and to our knowledge
only on the postsynaptic side. Furthermore, ACh/DA interactions and their relationships with
the symptomatology of DLB and related pathologies (PDD) had never been investigated.
Status | Completed |
Enrollment | 34 |
Est. completion date | October 2013 |
Est. primary completion date | September 2013 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years to 90 Years |
Eligibility |
Inclusion Criteria: - Patients: man or woman probable DLB, with and without extrapyramida syndrome - Healthy subjects: man or woman with no neuropsychiatric disorders Exclusion Criteria: - Diagnostic or therapeutic irradiation during the 12 months before SPECT imaging - Age less than 18 and more than 90 - Iodine sensibility - Brain-vascular disease, severe brain injury, type I and II diabetes mellitus, thyroid dysfunction, chronic alcoholism - Pregnant and breast feeding women, women in age to procreate - Impossibility to undergo MRI study (pace-maker, claustrophobia) - Persons under guardianship, outside state to express their assent or in emergency situation - Healthy subjects: cognitive impairment, dementia |
Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Health Services Research
Country | Name | City | State |
---|---|---|---|
France | Groupe Hospitalier Pellegrin - C.H.U. de Bordeaux | Bordeaux |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Bordeaux |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Binding Potential (BP) quantification of each radioligand | Day 1 ; Day 1 and between day 14 to 28 | No | |
Secondary | Ratio dopaminergic system/cholinergic system Binding Potential | Day 1 and between day 14 to 28 | No |
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