PHANTOM-S: The Pre-Hospital Acute Neurological Therapy and Optimization of Medical Care in Stroke Patients - Study

PHASE2CompletedINTERVENTIONAL
Enrollment

614

Participants

Timeline

Start Date

May 31, 2011

Primary Completion Date

January 31, 2013

Study Completion Date

May 31, 2013

Conditions
Acute Stroke
Interventions
OTHER

Stroke Emergency Mobile Unit (STEMO)

Patients treated in the STEMO may receive a CT-scan and point-of-care laboratory work up. This depends on the results of the neurological examination including assessment of medical history and the indication for scanning by the radiologist on call. In case of no contraindications patients with acute ischemic stroke will receive intravenous tissue Plasminogen Activator (0.9 mg/kg BW) according to the routine use of tissue Plasminogen Activator in Germany within 4.5 hours of symptom onset but with no formal upper age limit. (In other words, patients older than 80 years will not be excluded.) In case of increased INR and intracerebral hemorrhage patients will receive Prothrombin Complex Concentrate (PCC). All other indications will be treated according to national guidelines or as considered appropriate by the neurologist.

Trial Locations (1)

10117

Charite - Universitätsmedizin Berlin, Berlin

Sponsors
All Listed Sponsors
collaborator

Berlin Firebrigade

UNKNOWN

collaborator

MEYTEC GmbH

UNKNOWN

collaborator

B.R.A.H.M.S GmbH ThermoFisher Scientific

UNKNOWN

collaborator

Federal Ministry of Education and Research via Center for Stroke Research Berlin (CSB)

UNKNOWN

collaborator

European Union

OTHER

collaborator

Berlin Technology Foundation (EFRE)

UNKNOWN

collaborator

The Volkswagen Foundation

OTHER

collaborator

German Research Foundation

OTHER

lead

Charite University, Berlin, Germany

OTHER