Actively Recruiting

Age: 18Years +
All Genders
NCT03356392

German Stroke Registry - Endovascular Treatment

Led by Universitätsklinikum Hamburg-Eppendorf · Updated on 2024-12-11

10000

Participants Needed

1

Research Sites

626 weeks

Total Duration

On this page

Sponsors

U

Universitätsklinikum Hamburg-Eppendorf

Lead Sponsor

U

University Hospital of Cologne

Collaborating Sponsor

AI-Summary

What this Trial Is About

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

Official Title

German Stroke Registry - Endovascular Treatment

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 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
Not Eligible

You will not qualify if you...

  • None

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University Medical Center Hamburg-Eppendorf (UKE)

Hamburg, Free and Hanseatic City of Hamburg, Germany, 20251

Actively Recruiting

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Research Team

M

Maximilian Schell

CONTACT

G

Götz Thomalla, Prof. Dr. med.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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