Clinical trial

Evaluation of Circulating Exosomal MicroRNAs as Surrogate Stroke-Clock in Acute Anterior Circulation Large Vessel Occlusion

Name
HM20025643
Description
Patients \>18 years of age presenting to Ohio State Wexner Medical Center Emergency department with stroke symptoms, within 6 hours of last know well and found to have acute anterior circulation large vessel occlusion (LVO) will be included in this study. The purpose of this study is to evaluate the differential expression of exosomal microRNAs in patients with stroke due to acute LVO as compared to healthy controls. In addition, the investigators will also evaluate the differential expression of exosomal microRNA in patients with good vs poor collateral grade.
Trial arms
Trial start
2018-08-14
Estimated PCD
2024-06-21
Trial end
2024-06-21
Treatment
miRNA sampling
Blood samples for miRNA testing will be collected from all subjects (control and patients diagnosed with acute ischemic stroke)
Arms:
Control, Stroke
Size
45
Primary endpoint
identification of differentially expressed microRNAs in patients with sudden acute anterior circulation large vessel occlusion, compared to healthy controls.
2 years
Eligibility criteria
Inclusion criteria: 1. Age 18 years or older. 2. Diagnosis of Acute Ischemic Stroke secondary to LVO 3. LVO from presumed embolic source (\<50% ICA) 4. CT perfusion/RAPID images showing salvageable penumbra (evaluated by PI) Exclusion: 1. \>50% stenosis of internal carotid artery 2. \>50% stenosis of bilateral vertebral arteries. 3. Patients with moderate to severe intracranial atherosclerotic disease as seen in CTA of head and neck. 4. Known moderate to severe PVD or symptomatic CAD 5. Past medical history of stent or coronary artery bypass surgery 6. Prisoners 7. Pregnant women 8. Previous stroke within 30 days 9. Intracranial vascular malformation or evidence of moya-moya disease 10. Serious advanced or terminal illness per judgment of the investigator with life expectancy \<1yr 11. Known allergy to iodine that precludes CTA or CTP studies 12. Presumed septic embolus or suspected bacterial endocarditis
Protocol
{'studyType': 'OBSERVATIONAL', 'patientRegistry': False, 'designInfo': {'observationalModel': 'COHORT', 'timePerspective': 'PROSPECTIVE'}, 'bioSpec': {'retention': 'SAMPLES_WITHOUT_DNA', 'description': 'microRNA sampling'}, 'enrollmentInfo': {'count': 45, 'type': 'ESTIMATED'}}
Updated at
2024-05-07

1 organization

1 product

1 indication

Product
miRNA