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Florida Cerebrovascular Disease Biorepository and Genomics Center

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Mayo Clinic

Status

Enrolling

Conditions

Subarachnoid Hemorrhage
Non-Aneurysmal Perimesencephalic Subarachnoid Haemorrhage
Ischemic Stroke
Asymptomatic Carotid Artery Stenosis
Moyamoya Disease
Leukoaraiosis
Transient Ischemic Attack
Intracerebral Hemorrhage
Reversible Cerebral Vasoconstriction Syndrome
Arteriovenous Fistula
CADASIL
Anoxic Brain Injury
Cerebrovascular Disease
Aneurysmal Subarachnoid Hemorrhage
Vascular Dementia
Carotid Artery Stenosis Symptomatic
Fibromuscular Dysplasia
Cerebral Venous Thrombosis
Unruptured Intracranial Aneurysm

Study type

Observational

Funder types

Other

Identifiers

NCT05491980
22-002667

Details and patient eligibility

About

The purpose of this study is to create a state-wide biorepository and resource center for cerebrovascular diseases in Florida, which will include collecting medical history information and blood from subjects affected by cerebrovascular disease. The information and blood samples collected may be used in future research for the study of cerebrovascular disease and to learn about, prevent or treat other health problems.

Enrollment

5,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

• Affected subjects with diverse cerebrovascular conditions, including, but not limited to, ischemic stroke, transient ischemic attack (TIA), intracerebral hemorrhage (ICH), aneurysmal subarachnoid hemorrhage (aSAH), vascular dementia (VAD), anoxic brain injury, unruptured intracranial aneurysm (UIA), cavernous malformation, arteriovenous malformations (AVM), carotid and vertebral arterial dissections, symptomatic and asymptomatic cervical carotid artery atherosclerotic stenosis, non-aneurysmal perimesencephalic subarachnoid hemorrhage (naSAH), cerebral venous thrombosis (CVT), moyamoya disease, fibrosmuscular dysplasia (FMD), non-traumatic, angiography-negative subarachnoid hemorrhage, leukoaraiosis, arteriovenous fistula, reversible cerebral vasoconstriction syndrome (RCVS), and CADASIL.

Exclusion criteria

• All patients with the following known or suspected virulent microorganisms causing an active or latent infection will be excluded from the study:

  • Human immunodeficiency virus (HIV);
  • Any viral hepatitis;
  • West Nile virus (WNV);
  • Influenza virus;
  • Tuberculosis (TB);
  • Any bacteremia;
  • Any fungemia;
  • Any prionopathy.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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