Swiss Intravenous and Intra-arterial Thrombolysis for Treatment of Acute Ischemic Stroke Registry

NCT00811538 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1476

Last updated 2016-04-13

No results posted yet for this study

Summary

The clinical and radiological data of patients with an acute ischemic stroke treated with intravenous thrombolysis (IVT) or intraarterial thrombolysis (IAT) in a Swiss stroke unit are assessed in a Swiss Multicenter Thrombolysis Registry. Like in clinical routine, a clinical evaluation takes place in a 3-months follow-up. Furthermore quality of life is assessed with a standardized questionnaire. The aim of the registry is to compare the safety and efficacy of IVT and IAT in patients with acute ischemic stroke. The registry also helps to improve in-hospital-management of stroke patients.

Conditions

Interventions

PROCEDURE

Intravenous Thrombolysis

i.V. thrombolysis with rtPa

PROCEDURE

Intraarterial Thrombolysis

Endovascular treatment with i.a. Urokinase or i.a. rtPA or mechanical recanalization techniques

Sponsors & Collaborators

  • Swiss Heart Foundation

    collaborator OTHER
  • University of Zurich

    collaborator OTHER
  • University Hospital, Basel, Switzerland

    collaborator OTHER
  • University Hospital, Geneva

    collaborator OTHER
  • University of Lausanne Hospitals

    collaborator OTHER
  • Kantonsspital Aarau

    collaborator OTHER
  • Cantonal Hospital of St. Gallen

    collaborator OTHER
  • Triemli Hospital

    collaborator OTHER
  • Insel Gruppe AG, University Hospital Bern

    lead OTHER

Principal Investigators

  • Marcel Arnold, MD Prof. · Dep. of Neurology, Bern University Hospital, Switzerland

  • Krassen Nedeltechev, MD Prof. · Kantonsspital Aarau, Switzerland

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-12-31
Primary Completion
2015-03-31
Completion
2015-12-31

Countries

  • Switzerland

Study Locations

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Entities

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 NCT00811538 on ClinicalTrials.gov