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Prospective Cohort With Incident Stroke

NCT01364168 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 850

Last updated 2024-03-19

No results posted yet for this study

Summary

The primary aim of the study is to derive and validate risk scores for vascular endpoints (recurrent stroke, myocardial infarction, and other complications of stroke) and for death following an incident stroke. For this purpose patients with an incident stroke will be followed for 36 months with additional assessments at 3, 12, 24 and 36 months.

Conditions

Sponsors & Collaborators

  • Charite University, Berlin, Germany

    collaborator OTHER

  • Ludwig-Maximilians - University of Munich

    lead OTHER

Principal Investigators

  • Martin Dichgans, Prof. · Institute for Stroke and Dementia Research, Klinikum der Universität München

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-02-28
Primary Completion
2024-12-31
Completion
2027-12-31

Countries

  • Germany

Study Locations

More Related Trials

Entities

Diseases

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 NCT01364168 on ClinicalTrials.gov