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Information Recall on Informed Consent to Intravenous Thrombolysis in Patients With Acute Ischaemic Stroke.

NCT03246256 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 260

Last updated 2020-11-13

No results posted yet for this study

Summary

The aim of the study is to investigate the ability to recall information given during informed consent on intravenous thrombolysis in patients with acute ischaemic stroke.

Conditions

Interventions

OTHER

Group 1

Sponsors & Collaborators

  • Department of Neurology, Charité - Universitätsmedizin Berlin, Germany

    collaborator UNKNOWN

  • Department of Cardiology and Pneumology, Charité, Campus Benjamin Franklin

    collaborator UNKNOWN

  • Charite University, Berlin, Germany

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-12-21
Primary Completion
2020-06-30
Completion
2021-06-30

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 NCT03246256 on ClinicalTrials.gov