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Helsinki Ultra-acute Stroke Biomarker Study

H

Helsinki University Central Hospital (HUCH)

Status

Completed

Conditions

Acute Stroke

Study type

Observational

Funder types

Other

Identifiers

NCT02145663
MNEURT ISCHEMIC STROKE 813 (Other Identifier)
HUSBS2013

Details and patient eligibility

About

The aim of this study is to establish diagnostic and predictive biomarkers for patients with suspected acute stroke, that are transported by EMS as candidates for thrombolytic treatment. The study focuses on the ultra acute phase, <4.5 hours from symptom onset, including the prehospital setting. Analyses will include known biomarkers (e.g. GFAP, NR2 peptide) and a discovery phase for novel markers. Patient outcome will be evaluated at 3 month using the modified Rankin Scale (mRS).

Enrollment

1,046 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Acute stroke suspected by EMS personnel
  • Transport to tertiary hospital as possible candidate for thrombolytic treatment of ischemic stroke
  • Age ≥18
  • Successful prehospital blood sampling by EMS personnel

Exclusion criteria

  • Unsuccessful prehospital blood sampling by EMS personnel

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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