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German Stroke Registry - Endovascular Treatment

German Stroke Registry - Endovascular Treatment

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03356392
Acronym
GSR-ET
Enrollment
10000
Registered
2017-11-29
Start date
2015-06-30
Completion date
2027-06-30
Last updated
2024-12-11

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

Conditions

Acute Ischemic Stroke

Keywords

acute stroke, thrombectomy, endovascular treatment

Brief 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.

Interventions

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

Sponsors

University Hospital of Cologne
CollaboratorOTHER
Klinikum rechts der Isar, Technical University of Munich
CollaboratorUNKNOWN
RWTH Aachen University
CollaboratorOTHER
University Hospital Tuebingen
CollaboratorOTHER
Charite University, Berlin, Germany
CollaboratorOTHER
Charité - Universitätsmedizin Berlin, Campus Virchow Klinikum
CollaboratorUNKNOWN
Sana Klinikum Offenbach
CollaboratorOTHER
Goethe University
CollaboratorOTHER
Klinikum Dortmund
CollaboratorUNKNOWN
KRH Klinikum Nordstadt
CollaboratorUNKNOWN
Asklepios Klinik Altona
CollaboratorUNKNOWN
Klinikum Altenburger Land
CollaboratorUNKNOWN
Klinikum Stadt Hanau
CollaboratorOTHER
Klinikum Lüneburg
CollaboratorUNKNOWN
Ludwig-Maximilians - University of Munich
CollaboratorOTHER
University of Göttingen
CollaboratorOTHER
Krankenhaus Buchholz
CollaboratorUNKNOWN
Klinikum Osnabrück
CollaboratorUNKNOWN
Wuerzburg University Hospital
CollaboratorOTHER
University of Giessen and Marburg
CollaboratorUNKNOWN
Sana Kliniken Lübeck
CollaboratorUNKNOWN
Mühlenkreiskliniken Minden
CollaboratorUNKNOWN
radprax MVZ Nordrhein
CollaboratorUNKNOWN
University Hospital Muenster
CollaboratorOTHER
University Medical Center Rostock
CollaboratorOTHER
Asklepios Klinik Wandsbek
CollaboratorUNKNOWN
Elbe Kliniken
CollaboratorUNKNOWN
Städtische Klinikum Braunschweig
CollaboratorUNKNOWN
Allgemeines Krankenhaus Celle
CollaboratorUNKNOWN
Bezirkskrankenhaus Günzburg
CollaboratorUNKNOWN
Klinikum Bremen-Mitte, gGmbH
CollaboratorOTHER
University Medical Center Mainz
CollaboratorOTHER
Klinikum Köln-Merheim
CollaboratorUNKNOWN
University Hospital, Bonn
CollaboratorOTHER
Universitätsklinikum Hamburg-Eppendorf
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Clinical diagnosis of acute ischemic stroke * Eligible for intravenous thrombolysis (IVT) and IVT initiated within 4.5 hours after stroke onset * Confirmed diagnosis of persistent occlusion of terminal carotid artery, middle cerebral artery (M1 or M2), or basilar artery consistent with symptoms * Age \>18 years * Ethic approval in process

Exclusion criteria

none

Design outcomes

Primary

MeasureTime frameDescription
modified Ranking Scale (mRS) on day 9090 daysThe scale is a commonly used measurement for the degree of disability or dependence in the daily activities of people who have suffered a stroke; scale range 0-6; with 0 - No symptoms. 1 - No significant disability. Able to carry out all usual activities, despite some symptoms. 2 - Slight disability. Able to look after own affairs without assistance, but unable to carry out all previous activities. 3 - Moderate disability. Requires some help, but able to walk unassisted. 4 - Moderately severe disability. Unable to attend to own bodily needs without assistance, and unable to walk unassisted. 5 - Severe disability. Requires constant nursing care and attention, bedridden, incontinent. 6 - Dead. publication: van Swieten J, Koudstaal P, Visser M, Schouten H, et al. (1988). Interobserver agreement for the assessment of handicap in stroke patients. Stroke. 19 (5): 604-607. doi:10.1161/01.str.19.5.604. PMID 3363593.

Countries

Germany

Contacts

Primary ContactMaximilian Schell
m.schell@uke.de+49 (0)1522/2834807
Backup ContactGötz Thomalla, Prof. Dr. med.
thomalla@uke.de+49 (0)40/7410-0

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 13, 2026