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Evaluation of a Multimodal Neuroimaging Method for Diagnosis in Parkinsonian Syndromes

Evaluation and Validation of a Multimodal MRI Neuroimaging Method: Application to Differential Diagnosis and Disease Progression in Parkinsonian Syndromes

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02428816
Acronym
MultiPAMS
Enrollment
94
Registered
2015-04-29
Start date
2013-01-24
Completion date
2016-07-28
Last updated
2021-02-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple System Atrophy, Parkinson's Disease

Keywords

differential diagnosis, multimodal MRI, Parkinson's Disease, Multiple System Atrophy

Brief summary

Based on previous promising results, the next step for the validation of a multimodal MRI method in diagnosis and follow up of patients reached by parkinsonian syndromes is (i) to test whether the multimodal neuroimaging is able to discriminate at the individual level, patients with multiple system atrophy parkinsonism (MSA) and patients with idiopathic Parkinson's disease (PD) (ii) to determine whether the method is sensitive to measure changes over time for the two diseases, according to imaging, neuropsychological and other clinical data. Patients will be compared with healthy controls.

Detailed description

30 patients with PD, 30 patients with MSA and 30 healthy controls will be examined in a 3Tesla MRI. The aim of our project is to demonstrate that our multimodal MRI method can discriminate both diseases with a similar clinical presentation and monitor the progress of the disease. CIC's expertise in recruitment and assessment of patients, and the powers of the INSERM U825 in terms of development and processing in neuroimaging guarantee the feasibility of the project and its successful completion.

Interventions

MRI acquisitions

BEHAVIORALbehavioral evaluations

Evaluations about motor abilities, sleep, cognition and lifestyle

Sponsors

Institut National de la Santé Et de la Recherche Médicale, France
Lead SponsorOTHER_GOV

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* informed consent signed * right handed patients * Mini Mental Score \> 22 * no other neurological disease than Parkinson's Disease (PD) or Multiple System Atrophy (MSA) * non-demented patients reached by PD or MSA (according to diagnosis criteria from UK PD Brain Bank and from Gilman and colleagues, 1998, for PD and MSA respectively) * for PD patients only : Hoehn and Yahr score from 2 to 3

Exclusion criteria

* claustrophobia * contraindications to MRI (cardiac or auditive prothesis, pacemakers, cerebral clip, stimulating electrodes) * pregnant women * major neuropsychiatric disease * refusal to be informed in case of cerebral anomaly detected during MRI acquisition * uncompensated thyroid deficit

Design outcomes

Primary

MeasureTime frame
The primary outcome measure to discriminate individual patients and patients with MPI and AMS through multimodal MRI isolating multiparametric spatial signature resulting from a combination of markers in multimodal imaging.1 year

Secondary

MeasureTime frame
correlate MP and MSA disease severity with extracted multimodal MRI biomarkers in whole brain1 year

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026