German Stroke Registry - Endovascular Treatment

NCT03356392 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 10000

Last updated 2024-12-11

No results posted yet for this study

Summary

The German Stroke Registry (GSR) Endovascular Treatment is an academic, independent, prospective, multicentre, observational registry study. Consecutive patients treated with endovascular stroke treatment will be enrolled in German stroke centers. Patients receive regular care and data will be collected as part of clinical routine. Baseline clinical and procedural information as well clinical follow-up information during in-hospital stay, and up to 90 days of stroke onset are collected. Data collected include demographics, National Institute of Health Stroke Scale (NIHSS) on admission, pre-treatment ASPECTS, information on timing and success of interventional treatment, procedural complications, intracranial hemorrhage, and functional outcome.

Conditions

  • Acute Ischemic Stroke

Interventions

OTHER

telephone call d90

telephone call on day 90 to assess the primary outcome (mRs d90)

Sponsors & Collaborators

  • University Hospital of Cologne

    collaborator OTHER
  • Klinikum rechts der Isar, Technical University of Munich

    collaborator UNKNOWN
  • RWTH Aachen University

    collaborator OTHER
  • University Hospital Tuebingen

    collaborator OTHER
  • Charite University, Berlin, Germany

    collaborator OTHER
  • Charité - Universitätsmedizin Berlin, Campus Virchow Klinikum

    collaborator UNKNOWN
  • Sana Klinikum Offenbach

    collaborator OTHER
  • Goethe University

    collaborator OTHER
  • Klinikum Dortmund

    collaborator UNKNOWN
  • KRH Klinikum Nordstadt

    collaborator UNKNOWN
  • Asklepios Klinik Altona

    collaborator UNKNOWN
  • Klinikum Altenburger Land

    collaborator UNKNOWN
  • Klinikum Stadt Hanau

    collaborator OTHER
  • Klinikum Lüneburg

    collaborator UNKNOWN
  • Ludwig-Maximilians - University of Munich

    collaborator OTHER
  • University of Göttingen

    collaborator OTHER
  • Krankenhaus Buchholz

    collaborator UNKNOWN
  • Klinikum Osnabrück

    collaborator UNKNOWN
  • Wuerzburg University Hospital

    collaborator OTHER
  • University of Giessen and Marburg

    collaborator UNKNOWN
  • Sana Kliniken Lübeck

    collaborator UNKNOWN
  • Mühlenkreiskliniken Minden

    collaborator UNKNOWN
  • radprax MVZ Nordrhein

    collaborator UNKNOWN
  • University Hospital Muenster

    collaborator OTHER
  • University Medical Center Rostock

    collaborator OTHER
  • Asklepios Klinik Wandsbek

    collaborator UNKNOWN
  • Elbe Kliniken

    collaborator UNKNOWN
  • Städtische Klinikum Braunschweig

    collaborator UNKNOWN
  • Allgemeines Krankenhaus Celle

    collaborator UNKNOWN
  • Bezirkskrankenhaus Günzburg

    collaborator UNKNOWN
  • Klinikum Bremen-Mitte, gGmbH

    collaborator OTHER
  • University Medical Center Mainz

    collaborator OTHER
  • Klinikum Köln-Merheim

    collaborator UNKNOWN
  • University Hospital, Bonn

    collaborator OTHER
  • Universitätsklinikum Hamburg-Eppendorf

    lead OTHER

Principal Investigators

  • Martin Dichgans, Prof. Dr. med. · LMU, Munich, Germany

  • Christian Gerloff, Prof. Dr. med. · UKE, Hamburg, Germany

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-06-30
Primary Completion
2027-06-30
Completion
2027-06-30

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03356392 on ClinicalTrials.gov