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UnknownNCT03022357

Nigrosomal Iron Imaging in Parkinson's Disease

Status
Unknown
Phase
Study type
Observational
Enrollment
145 (estimated)
Sponsor
University of Nottingham · Academic / Other
Sex
All
Age
21 Years – 90 Years
Healthy volunteers
Not accepted

Summary

Prospective observational study to compare sensitivity of 3T functional Magnetic Resonance Imaging (3T fMRI) at diagnosing Parkinson's Disease (PD) against the benchmark DaTScan diagnostic test and clinical diagnosis at follow up.

Detailed description

Idiopathic Parkinson's is characterized by loss of midbrain dopaminergic neurons preferentially affecting the nigrosomes of the pars compacta of the substantia nigra (SNpc). At the time of clinical diagnosis, an estimated 50-70% of the neurons of the SNpc are lost. Non-invasive imaging of cell loss in the nigrosomes containing the SNpc dopaminergic neurons would be clinically desirable for accurate diagnosis in clinically uncertain cases of parkinsonism, especially in the early stages of Parkinson's. Investigators recently discovered that high resolution susceptibility weighted MRI at 7T and 3T demonstrates iron related signal loss of the NS1 in Parkinson's. These studies proved the feasibility and potential of in vivo nigrosome MRI as new diagnostic tool for Parkinson's. Further support of and confidence in our novel diagnostic concept comes from similar observations by other research groups. Project goals To establish whether nigrosome MRI is an alternative to DatScanTM in the diagnosis of early Parkinson's in patients with diagnostic uncertainty. To establish whether nigrosomal iron predicts the severity of Parkinson's. As a secondary aim the investigators will study if nigrosomal iron load as determined by susceptometry correlates to disease severity (MDS-UPDRS). TRIAL / STUDY OBJECTIVES AND PURPOSE PURPOSE * To establish whether nigrosome MRI is an alternative to DatScan in the diagnosis of early Parkinson's * To establish whether nigrosomal iron predicts the severity of Parkinson's. PRIMARY OBJECTIVE Validation of NS1 MRI as a qualitative diagnostic marker in early Parkinson's • To investigate whether the presence or absence of the swallow tail on nigrosome MRI at 3T is as accurate as DatScan and at least 80% sensitive and 80% specific to predict the final clinical diagnosis of Parkinson's vs. other movement disorder in patients with indeterminate or atypical parkinsonian features. Hypothesis 1: That the swallow tail sign is an accurate marker of early Parkinson's SECONDARY OBJECTIVES Biomarker discovery based on quantitative nigrosome iron markers in Parkinson's • To investigate whether diagnostic performance of nigrosome MRI can be further improved through quantitative assessment of nigrosomal iron and combination with neuromelanin metrics. Hypothesis 2: That nigrosomal iron metrics further improve the detection of early Parkinson's • To assess how well disease severity can be predicted by iron content in the nigrosome and by a combination of iron content and the size of the neuromelanin-rich nigra volume. Hypothesis 3: That nigrosomal iron metrics are closely associated with severity of early Parkinson's The investigators will be recruiting 145 patients with diagnostic uncertainty of Parkinson's Disease. These patients will undergo a MRI and DATscans and will be clinically examined. They will then be followed-up (clinical examination) in 12 months, identifying if they can be confirmed as having Parkinson's Disease, in order to compare the sensitivity and specificity of nigrosome1 detected by MRI with DATScan, potentially allowing a non-invasive and much less expensive means of diagnosing Parkinson's Disease.

Conditions

Interventions

TypeNameDescription
OTHERPatient assessmentClinical examination, Examination, Questionnaires
RADIATIONDATScanIn small subgroup
RADIATIONOrbital X-RayIf foreign body in eye needs exclusion
OTHERMagnetic Resonance Imaging (MRI)MRI scanning of all subjects

Timeline

Start date
2016-06-01
Primary completion
2019-04-01
Completion
2019-05-01
First posted
2017-01-16
Last updated
2018-10-12

Locations

3 sites across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT03022357. Inclusion in this directory is not an endorsement.