Percutaneous Recanalization in Ischemic Stroke Management in Europe Observational Registry

NCT01560247 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2012-04-05

No results posted yet for this study

Summary

To determine the revascularization rate, clinical efficacy and safety of the CE-marked MindFrame System in ischemic stroke patients

Conditions

Interventions

PROCEDURE

Mechanical thrombectomy

Mechanical thrombectomy using a MindFrame device

Sponsors & Collaborators

  • MindFrame, Inc.

    lead INDUSTRY

Principal Investigators

  • Michael Soderman, MD, PhD · Karolinska Institutet

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-01-31
Primary Completion
2014-09-30
Completion
2014-12-31

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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 NCT01560247 on ClinicalTrials.gov