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Comparative analysis of stroke care with and without a mobile stroke unit (MSU) in Mannheim

Comparative analysis of stroke care with and without a mobile stroke unit (MSU) in Mannheim

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00039715
Enrollment
240
Registered
2026-04-17
Start date
2026-04-28
Completion date
Unknown
Last updated
2026-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute stroke I63

Interventions

Group 1: Arm 1: Mobile Stroke Unit (MSU) Prehospital neurological assessment and acute stroke care delivered by the Mobile Stroke Unit during its operational hours. This includes an initial clinical-n

Sponsors

Neurologische Klinik und Klinik für Radiologie und Nuklearmedizin, Universitätsmedizin Mannheim Universitätsklinikum Mannheim GmbH Medizinische Fakultät Mannheim der Universität Heidelberg
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Suspected acute stroke, identified either by the Integrated Dispatch Center Mannheim or by emergency medical personnel. - Primary care provided in Mannheim either by the Mobile Stroke Unit (MSU) during its operational hours or by the conventional emergency medical service (non-MSU) when the MSU is not available. - Final diagnosis of a cerebrovascular event (e.g., ischemic stroke, intracerebral hemorrhage, transient ischemic attack). - Treatment at the University Medical Center Mannheim with complete clinical baseline documentation.

Exclusion criteria

Exclusion criteria: - No final diagnosis of a cerebrovascular event (e.g., differential diagnoses such as migraine, epileptic seizure without stroke, or hypoglycemia). - No treatment or diagnostic work-up at the University Medical Center Mannheim (no access to complete routine clinical data). - Technically or organizationally incomplete documentation that does not allow assessment of the primary endpoints.

Design outcomes

Primary

MeasureTime frame
Reduction of time-critical process intervals in acute stroke care. The following metrics will be collected in the MSU and will be compared between the MSU and non-MSU groups: Onset-to-Imaging time (time from symptom onset/“last seen well” to first brain imaging), Onset-to-Needle time (time to initiation of intravenous thrombolysis), Onset-to-Groin time (time to arterial puncture for mechanical thrombectomy), Onset-to-Stroke Unit time (time to admission to the Stroke Unit)

Secondary

MeasureTime frame
Functional outcome (Modified Rankin Scale at discharge and at three months), neurological severity (National Institutes of Health Stroke Scale at admission, after treatment, and at discharge), quality of life (patient-reported outcome measures at the three-month follow-up), complication rates (including symptomatic intracranial hemorrhage and other therapy-associated complications), and in-hospital care parameters (length of hospital and ward stay, rate of emergency department bypass), assessed from post-discharge medical records or via telephone follow-up.

Countries

Germany

Contacts

Public ContactCarolin Hoyer

Neurologische Klinik, Universitätsmedizin Mannheim Universitätsklinikum Mannheim GmbH Medizinische Fakultät Mannheim der Universität Heidelberg

carolin.hoyer@umm.de+496213832213

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Jun 11, 2026