Copeptin for Risk Stratification in Acute Stroke Patients: the CoRisk Study
NCT00878813 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1102
Last updated 2011-11-10
Summary
Prospective observational multicenter study to evaluate copeptin as a prognostic marker in patients with an acute cerebrovascular event. It includes four groups of patients, mainly depending on type of initial therapy (intra-arterial thrombolysis, intravenous thrombolysis, conservative treatment, TIA). The study takes place at the Emergency and neurological Department of the University of Bern, Switzerland; Department of Neurology, Goethe University of Frankfurt a.M. (Germany). Further participating centers are under discussion
Conditions
- Stroke
- Transient Ischemic Attack
Interventions
- PROCEDURE
-
Sampling of 15ml blood
On admission, 2 x 7.5ml blood tubes will be drawn during the first routine blood sampling
- PROCEDURE
-
Blood-Sampling
On day 1 after intra-arterial thrombolysis, 2 x 7.5ml blood tubes on the following routine blood-sampling will be drawn.
Sponsors & Collaborators
-
University of Basel
collaborator OTHER -
Charite University, Berlin, Germany
collaborator OTHER -
Goethe University
collaborator OTHER -
Insel Gruppe AG, University Hospital Bern
lead OTHER
Principal Investigators
-
Gian Marco De Marchis, MD · Inselspital, Bern University Hospital
-
Marcel Arnold, MD · Inselspital, Bern University Hospital
-
Mira Katan, MD · University Hospital, Basel, Switzerland
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2009-03-31
- Primary Completion
- 2011-04-30
- Completion
- 2011-10-31
Countries
- Germany
- Switzerland
Study Locations
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