Vessel Wall Imaging for Diagnosis and Monitoring of Central Nervous System (CNS) Vasculitis
Primary Purpose
Vasculitis, CNS, Vasculitis, Cerebral
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
MRI, including intracranial vessel wall imaging
Sponsored by
About this trial
This is an interventional diagnostic trial for Vasculitis, CNS
Eligibility Criteria
Inclusion Criteria:
- 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.
- Ability to undergo routine clinical testing, including lumbar puncture performed for PACNS to exclude potential alternative diagnoses (for initial suspected cases).
- Ability to provide informed consent.
Exclusion Criteria:
- Less than 18 years of age.
- Any absolute contraindication to 3 Tesla MRI.
- Any absolute contraindication to gadolinium.
- Contraindication to lumbar puncture such as severe coagulopathy.
- High risk carotid atherosclerotic plaque defined as either greater than 70% stenosis or known high risk plaque features such as intra-plaque hemorrhage.
- Medium or high risk factors for cardioembolic stroke based on the Trial of Org 10172 in Acute Stroke Treatment (TOAST) criteria.
Sites / Locations
- Mayo Clinic
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Suspected CNS Vasculitis
Arm Description
Patients with suspected CNS vasculitis will undergo an MRI, including intracranial vessel wall imaging.
Outcomes
Primary Outcome Measures
Number of Subjects with Diagnosis of Stroke
Clinical or MRI evidence of stroke on follow-up exam.
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03166319
Brief Title
Vessel Wall Imaging for Diagnosis and Monitoring of Central Nervous System (CNS) Vasculitis
Official Title
The Utility of Intracranial Vessel Wall Imaging for Suspected CNS Vasculitis Diagnosis and Assessment of Disease Activity.
Study Type
Interventional
2. Study Status
Record Verification Date
March 2022
Overall Recruitment Status
Completed
Study Start Date
July 24, 2017 (Actual)
Primary Completion Date
November 24, 2020 (Actual)
Study Completion Date
November 24, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mayo Clinic
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
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.
Detailed Description
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;
A specific clinical and pathologic subtype of PACNS,
PACNS not otherwise specified (NOS) without pathologic or clinical proof of a specific subtype, or
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vasculitis, CNS, Vasculitis, Cerebral
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Patients with suspected primary CNS vasculitis.
Masking
None (Open Label)
Allocation
N/A
Enrollment
15 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Suspected CNS Vasculitis
Arm Type
Experimental
Arm Description
Patients with suspected CNS vasculitis will undergo an MRI, including intracranial vessel wall imaging.
Intervention Type
Diagnostic Test
Intervention Name(s)
MRI, including intracranial vessel wall imaging
Intervention Description
MRI/MRA/intracranial high-resolution vessel wall imaging (HR-VWI)
Primary Outcome Measure Information:
Title
Number of Subjects with Diagnosis of Stroke
Description
Clinical or MRI evidence of stroke on follow-up exam.
Time Frame
Approximately 5 months after baseline
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
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.
Ability to undergo routine clinical testing, including lumbar puncture performed for PACNS to exclude potential alternative diagnoses (for initial suspected cases).
Ability to provide informed consent.
Exclusion Criteria:
Less than 18 years of age.
Any absolute contraindication to 3 Tesla MRI.
Any absolute contraindication to gadolinium.
Contraindication to lumbar puncture such as severe coagulopathy.
High risk carotid atherosclerotic plaque defined as either greater than 70% stenosis or known high risk plaque features such as intra-plaque hemorrhage.
Medium or high risk factors for cardioembolic stroke based on the Trial of Org 10172 in Acute Stroke Treatment (TOAST) criteria.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vance Lehman, MD
Organizational Affiliation
Mayo Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mayo Clinic
City
Rochester
State/Province
Minnesota
ZIP/Postal Code
55902
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Links:
URL
https://www.mayo.edu/research/clinical-trials
Description
Mayo Clinic Clinical Trials
Learn more about this trial
Vessel Wall Imaging for Diagnosis and Monitoring of Central Nervous System (CNS) Vasculitis
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