NCT05491980

Brief Summary

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.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
72

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Aug 2022

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 2, 2022

Completed
3 days until next milestone

First Submitted

Initial submission to the registry

August 5, 2022

Completed
3 days until next milestone

First Posted

Study publicly available on registry

August 8, 2022

Completed
3.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2026

Completed
Last Updated

March 23, 2026

Status Verified

March 1, 2026

Enrollment Period

3.7 years

First QC Date

August 5, 2022

Last Update Submit

March 19, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Stroke or TIA at 12 months

    Number of participants to experience new diagnosis of TIA or stroke.

    1 year

Secondary Outcomes (1)

  • Modified Rankin Scale

    1 year

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Subjects identified with a history of cerebrovascular disease will be recruited from both the in-patient and outpatient services at Mayo Clinic Florida.

You may qualify if:

  • 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.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Mayo Clinic Florida

Jacksonville, Florida, 32224, United States

Location

Related Links

MeSH Terms

Conditions

Cerebrovascular DisordersIschemic StrokeIschemic Attack, TransientCerebral HemorrhageSubarachnoid HemorrhageDementia, VascularHypoxia-Ischemia, BrainIntracranial ThrombosisMoyamoya DiseaseFibromuscular DysplasiaLeukoaraiosisArteriovenous FistulaCADASIL

Condition Hierarchy (Ancestors)

Brain DiseasesCentral Nervous System DiseasesNervous System DiseasesVascular DiseasesCardiovascular DiseasesStrokeBrain IschemiaIntracranial HemorrhagesHemorrhagePathologic ProcessesPathological Conditions, Signs and SymptomsIntracranial ArteriosclerosisIntracranial Arterial DiseasesDementiaLeukoencephalopathiesArteriosclerosisArterial Occlusive DiseasesNeurocognitive DisordersMental DisordersHypoxia, BrainHypoxiaSigns and Symptoms, RespiratorySigns and SymptomsIntracranial Embolism and ThrombosisThromboembolismEmbolism and ThrombosisCarotid Artery DiseasesCerebral Arterial DiseasesArteriovenous MalformationsVascular MalformationsCardiovascular AbnormalitiesVascular FistulaCongenital AbnormalitiesCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesFistulaPathological Conditions, AnatomicalCerebral InfarctionBrain InfarctionCerebral Small Vessel DiseasesGenetic Diseases, InbornInfarctionIschemiaNecrosis

Study Officials

  • James Meschia, MD

    Mayo Clinic

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

August 5, 2022

First Posted

August 8, 2022

Study Start

August 2, 2022

Primary Completion

April 1, 2026

Study Completion

April 1, 2026

Last Updated

March 23, 2026

Record last verified: 2026-03

Data Sharing

IPD Sharing
Will not share

Locations