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Safety and Performance Evaluation of the Magneto Wire

NCT03890380 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 4

Last updated 2020-07-07

No results posted yet for this study

Summary

A prospective, open label single arm feasibility study to evaluate the safety and performance of the Magneto Wire in patients diagnosed with acute ischemic stroke and planned for thrombectomy procedure.

Conditions

Interventions

DEVICE

Magneto Wire

Patients will be treated with Magneto Wire

Sponsors & Collaborators

  • Magneto Thrombectomy Solutions

    lead INDUSTRY

Principal Investigators

  • Shally Sharon · Magneto Thrombectomy Solutions

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-12-17
Primary Completion
2019-07-18
Completion
2019-10-27

Countries

  • Israel

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 NCT03890380 on ClinicalTrials.gov