Vessel Wall Imaging for Diagnosis and Monitoring of Central Nervous System (CNS) Vasculitis
Status: | Recruiting |
---|---|
Conditions: | Cardiology |
Therapuetic Areas: | Cardiology / Vascular Diseases |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 12/12/2018 |
Start Date: | July 24, 2017 |
End Date: | May 1, 2020 |
Contact: | Caleb Hammel |
Email: | hammel.caleb@mayo.edu |
Phone: | 507-293-0925 |
The Utility of Intracranial Vessel Wall Imaging for Suspected CNS Vasculitis Diagnosis and Assessment of Disease Activity.
This is a prospective pilot study to determine the utility of MRI and high resolution
intracranial vessel wall imaging for the diagnosis and disease activity assessment of
intracranial vasculitis.
intracranial vessel wall imaging for the diagnosis and disease activity assessment of
intracranial vasculitis.
This study will evaluate patients with suspected primary angiitis of the central nervous
system (PACNS), recruited during initial work-up by our multi-disciplinary team. Given the
low incidence of CNS vasculitis and the fact that some patients are routed to a quaternary
care center after initial work-up and diagnosis, evaluation of both groups will be useful to
maximize the number of participants evaluated and to provide a representative sample of
patients typically treated. During the study, participants will ultimately be deemed to have;
1. A specific clinical and pathologic subtype of PACNS,
2. PACNS not otherwise specified (NOS) without pathologic or clinical proof of a specific
subtype, or
3. An alternative diagnosis other than PACNS.
Patients will undergo a standardized imaging and clinical examination at presentation and at
pre-defined follow-up periods. Imaging examinations will include an MRI of the head, standard
magnetic resonance angiogram (MRA) of the head, and intracranial vessel wall imaging without
and with IV gadolinium. Patients will receive up to 4 imaging examinations at predefined
intervals as part of this study. MRI/MRA/Vessel wall features will be evaluated by 2
neuroradiologists. Imaging findings will be correlated to clinical and any available
laboratory or pathologic data. The target accrual is 10 patients for this pilot study.
system (PACNS), recruited during initial work-up by our multi-disciplinary team. Given the
low incidence of CNS vasculitis and the fact that some patients are routed to a quaternary
care center after initial work-up and diagnosis, evaluation of both groups will be useful to
maximize the number of participants evaluated and to provide a representative sample of
patients typically treated. During the study, participants will ultimately be deemed to have;
1. A specific clinical and pathologic subtype of PACNS,
2. PACNS not otherwise specified (NOS) without pathologic or clinical proof of a specific
subtype, or
3. An alternative diagnosis other than PACNS.
Patients will undergo a standardized imaging and clinical examination at presentation and at
pre-defined follow-up periods. Imaging examinations will include an MRI of the head, standard
magnetic resonance angiogram (MRA) of the head, and intracranial vessel wall imaging without
and with IV gadolinium. Patients will receive up to 4 imaging examinations at predefined
intervals as part of this study. MRI/MRA/Vessel wall features will be evaluated by 2
neuroradiologists. Imaging findings will be correlated to clinical and any available
laboratory or pathologic data. The target accrual is 10 patients for this pilot study.
Inclusion Criteria:
1. The patient is determined to have suspected PACNS upon evaluation by a neurologist or
rheumatologist or may have an established diagnosis of PACNS of any duration as
determined by a neurologist or rheumatologist.
2. Ability to undergo routine clinical testing, including lumbar puncture performed for
PACNS to exclude potential alternative diagnoses (for initial suspected cases).
3. Ability to provide informed consent.
Exclusion Criteria:
1. Less than 18 years of age.
2. Any absolute contraindication to 3 Tesla MRI.
3. Any absolute contraindication to gadolinium.
4. Contraindication to lumbar puncture such as severe coagulopathy.
5. High risk carotid atherosclerotic plaque defined as either greater than 70% stenosis
or known high risk plaque features such as intra-plaque hemorrhage.
6. Medium or high risk factors for cardioembolic stroke based on the Trial of Org 10172
in Acute Stroke Treatment (TOAST) criteria.
We found this trial at
1
site
Rochester, Minnesota 55905
Principal Investigator: Vance Lehman, MD
Phone: 507-293-0925
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