REal-World Analyses of Stroke - Thrombus Occlusion REtrieval

NCT04451525 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 710

Last updated 2025-06-18

No results posted yet for this study

Summary

To collect real-world evidence allowing assessment of functional, imaging, and safety outcomes of MicroVention market-released acute ischemic stroke devices when used at the direction of the treating physician.

Conditions

  • Acute Ischemic Stroke
  • Vessel Occlusion
  • Stroke
  • Ischemic

Interventions

DEVICE

MicroVention Mechanical Thrombectomy Devices as first-line treatment

Patient will be treated with mechanical thrombectomy at the direction of the treating physician

Sponsors & Collaborators

  • Microvention-Terumo, Inc.

    lead INDUSTRY

Principal Investigators

  • Dheeraj Gandhi, MBBS, MD · University of Maryland, Baltimore

  • Syed Zaidi, MD · ProMedica Toledo

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-07-15
Primary Completion
2025-05-29
Completion
2025-06-09
FDA Device
Yes

Countries

  • United States

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 NCT04451525 on ClinicalTrials.gov