Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
1040 participants
OBSERVATIONAL
2020-05-22
2026-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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CA (non-CASH)
Cavernous Angioma (CA) without symptomatic hemorrhage cases scheduled for evaluation by their neurology or neurosurgery teams in an inpatient or outpatient setting
observational
There is no intervention for any group in this observational study.
CA (CASH)
Cavernous Angioma (CA) with Symptomatic Hemorrhage (SH) cases scheduled for evaluation by their neurology or neurosurgery teams in an inpatient or outpatient setting
observational
There is no intervention for any group in this observational study.
Young with seizure
Young (\<30 years old) healthy control cohorts with seizures in the prior year
observational
There is no intervention for any group in this observational study.
Young without seizure
Young (\<30 years old) healthy control cohorts without seizures in the prior year
observational
There is no intervention for any group in this observational study.
Older with HMA
Older (\>50 years old) with hemorrhagic microangiopathy (HMA)
observational
There is no intervention for any group in this observational study.
Older without HMA
Older (\>50 years old) without hemorrhagic microangiopathy (HMA)
observational
There is no intervention for any group in this observational study.
Interventions
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observational
There is no intervention for any group in this observational study.
Eligibility Criteria
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Inclusion Criteria
2. age 18 or older
3. solitary or multiple
4. familial or sporadic
5. with or without prior symptoms
1. \< 30 years of age
2. one or more seizures (with or without medical therapy) in the prior year
OR
1. \> 50 years of age
2. having received an MRI of the brain with SWI (susceptibility weighted imaging) sequences for any indication in the year prior to enrollment
3. No HMA on brain MRI SWI sequences
OR
1. \> 50 years of age
2. having received an MRI of the brain with SWI sequences for any indication in the year prior to enrollment
3. Two or more microbleeds on SWI brain MRI sequences, adjudicated by neuroradiologist
Exclusion Criteria
2. prior stereotactic radiosurgery or any brain irradiation
3. spinal cavernoma without brain lesion
4. other brain pathology unrelated to CA (demyelinating disease, brain tumor)
5. seizures or stroke unrelated to CA in the prior year
6. current pregnancy or within 6 months postpartum
7. reluctance to undergo venipuncture or donate blood specimen, or be called for clinical follow-up for up to one year
8. homeless or incarcerated persons, or other reason a subject will be unable/unlikely to be reached for follow-up
Aim 3:
1. concurrent brain disease or structural brain pathology
2. medical illness requiring hospitalization or surgery, seizure or stroke in the prior 12 months
3. active use of prescription medications in the prior 12 months
4. current pregnancy or within 6 months postpartum
5. reluctance to undergo venipuncture or donate blood specimen
OR
1. concurrent brain disease or structural brain pathology
2. medical illness requiring hospitalization or surgery, or stroke in the prior 12 months other than seizure disorder
3. active use of prescription medications in the prior 12 months except anticonvulsants
4. current pregnancy or within 6 months postpartum
5. reluctance to undergo venipuncture or donate blood specimen
OR
1. concurrent brain disease or structural brain pathology
2. medical illness requiring hospitalization or surgery within the prior year
3. any history of stroke or epileptic seizure within the prior year
4. current pregnancy or within 6 months postpartum
5. reluctance to undergo venipuncture or donate blood specimen
OR
1. concurrent brain disease or structural brain pathology
2. medical illness requiring hospitalization or surgery within the prior year
3. any history of stroke or epileptic seizure within the prior year
4. current pregnancy or within 6 months postpartum
5. reluctance to undergo venipuncture or donate blood specimen
18 Years
ALL
Yes
Sponsors
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Mayo Clinic
OTHER
University of California, San Francisco
OTHER
National Institute of Neurological Disorders and Stroke (NINDS)
NIH
Barrow Neurological Institute
OTHER
University of Chicago
OTHER
Responsible Party
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Principal Investigators
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Issam Awad, MD
Role: PRINCIPAL_INVESTIGATOR
University of Chicago
Locations
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Barrow Neurological Institute at St. Joseph's Hospital and Medical Center
Phoenix, Arizona, United States
University of California, San Francisco
San Francisco, California, United States
The University of Chicago Medical Center
Chicago, Illinois, United States
Mayo Clinic
Rochester, Minnesota, United States
Countries
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References
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Girard R, Li Y, Stadnik A, Shenkar R, Hobson N, Romanos S, Srinath A, Moore T, Lightle R, Shkoukani A, Akers A, Carroll T, Christoforidis GA, Koenig JI, Lee C, Piedad K, Greenberg SM, Kim H, Flemming KD, Ji Y, Awad IA. A Roadmap for Developing Plasma Diagnostic and Prognostic Biomarkers of Cerebral Cavernous Angioma With Symptomatic Hemorrhage (CASH). Neurosurgery. 2021 Feb 16;88(3):686-697. doi: 10.1093/neuros/nyaa478.
Other Identifiers
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IRB20-0518
Identifier Type: -
Identifier Source: org_study_id
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