Status:

RECRUITING

Translational Immunodiagnostics in Stroke (TrImS)

Lead Sponsor:

The University of Hong Kong

Conditions:

Acute Ischemic Stroke

Haemorrhagic Stroke

Eligibility:

All Genders

18-100 years

Brief Summary

In adult patients presenting to emergency departments within 24 hours of symptom onset with suspected acute stroke, we aim: 1. to identify early brain- and pathology-specific circulating, whole blood...

Detailed Description

Introduction Stroke is a leading cause of overall mortality, morbidity and disability worldwide. In 2010 it was the second leading cause of death whilst in 2019 it ranked third overall for disability...

Eligibility Criteria

Inclusion

  • Patients eligible for enrolment include:
  • Adults ≥18 years of age.
  • Suspected acute stroke. Defined as either FAST-positive, or LAPSS-positive or ROSIER\>0
  • Within 24 hours of symptom onset.
  • Informed consent.
  • Control subjects will be drawn from two groups:
  • Non-neurologic patients who are matched with TIA and stroke cases (AIS, HS) for age, race, gender and smoking plus one or more of the following vascular risk factors: diabetes, hypertension, atrial fibrillation, hyperlipidaemia.
  • Relatives or accompanying friends.
  • Note that we will include and collect samples from the following cases if they present as suspected stroke and are recruited \<24 hours from symptom onset.
  • Any central nervous system infection, i.e. meningitis or encephalitis in the past 30 days
  • Any form of head trauma, stroke or intracranial haemorrhage in the past 30 days
  • Known primary or metastatic cancer involving the brain
  • Active cancer is defined as a diagnosis of cancer, within 6 months before enrollment, any treatment for cancer within the previous 6 months, or recurrent or metastatic cancer.
  • Autoimmune diseases: such as lupus, rheumatoid arthritis, Crohn's disease, ulcerative colitis
  • Active infectious diseases (e.g. HIV/AIDS, hepatitis C)
  • Major surgery within three months prior to the index event

Exclusion

  • Clear onset of acute symptoms \>24 hours.

Key Trial Info

Start Date :

May 1 2022

Trial Type :

OBSERVATIONAL

Allocation :

ESTIMATED

End Date :

May 30 2025

Estimated Enrollment :

650 Patients enrolled

Trial Details

Trial ID

NCT05300997

Start Date

May 1 2022

End Date

May 30 2025

Last Update

June 3 2024

Active Locations (1)

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Hong Kong University

Hong Kong, China