Natural History and Disease Progression Biomarkers of Multiple System Atrophy
NCT04229173 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 61
Last updated 2023-06-22
Summary
Multiple system atrophy (MSA) is a rare and fatal neurodegenerative disease characterised by a variable combination of parkinsonism, cerebellar impairment and autonomic dysfunction. The neuropathological hallmark is the accumulation of alpha-synuclein in oligodendrocytes. While some symptomatic treatments exist, neuroprotective treatments for MSA remain an urgent, unmet need. Moreover, at present there is not a single surrogate biomarker of MSA which could be used to inform clinical trials.
This study seeks to characterise the natural history of MSA on a panel of candidate biomarkers, pre-selected for being putative surrogates of the underlying neurodegenerative process
Conditions
Interventions
- DIAGNOSTIC_TEST
-
MRI acquisition
MRI acquisition
- DIAGNOSTIC_TEST
-
DAT-SPECT
Imaging with DAT SPECT (Dopamine Transporter, Single Photon Emission Computed Tomography)
- DIAGNOSTIC_TEST
-
blood sample, cerebrospinal fluid (optional)
blood sample, cerebrospinal fluid
- BEHAVIORAL
-
Evaluations about motor abilities, depression, cognition and lifestyle
Evaluations about motor abilities (UMSAR scale), depression (BDI scale), cognition (MoCA scale) and lifestyle (MSA- QoL)
- BEHAVIORAL
-
Evaluation about depression cognition
Evaluations about depression (BDI scale), cognition (MoCA scale)
Sponsors & Collaborators
-
University Hospital, Toulouse
lead OTHER
Principal Investigators
-
Olivier RASCOL, MD, PhD · University Hospital, Toulouse
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- OTHER
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 30 Years
- Max Age
- 80 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2020-05-26
- Primary Completion
- 2022-05-30
- Completion
- 2022-10-28
Countries
- France
Study Locations
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