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NCT04466033Completed

Evaluation of the Safety and Performance of Magneto Microcatheter

Evaluation of the Safety and Performance of Magneto Microcatheter for Endovascular Thrombectomy in Patients With Acute Ischemic Stroke

Source: ClinicalTrials.gov · Last updated 7 May 2025

Brief summary (registry, in English)

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

Status (registry)
Completed
Study type
Interventional
Enrollment
4 (actual)
First submitted
5 Jul 2020
Start date
1 Nov 2020
Primary completion date
1 Apr 2024
Lead sponsor
Magneto Thrombectomy Solutions
Diseases
Stroke
NCT number
NCT04466033

What you commit to

  • Study type: Interventional
  • Participants enrolled: 4
  • From 1 Nov 2020 to the primary completion date, 1 Apr 2024
  • 3 sites in 2 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Known bleeding diathesis
  • Uncontrolled hypertension (Systolic blood pressure\>185 or Diastolic blood pressure\>110) refractory to pharmacological management
  • CT scan or MRI with evidence of acute intracranial hemorrhage, ASPECT score\<6, mass effect and/or intracranial tumor
  • Angiographic evidence of either carotid dissection or vasculitis at the target site or any condition that may limit device access to the target site (i.e high grade stenosis) per the treating physician's discretion.

Lab values

  • Current use of oral anticoagulants with International Normalized Ratio (INR) \> 3;
  • PTT (Partial Thromboplastin Time)\>2 at screening

Other

  • Known use of cocaine or other vasoactive substance
  • Any known hemorrhagic or coagulation deficiency.
  • Pregnant or lactating female

Who the study is looking for

  • Clinical signs consistent with acute ischemic stroke
  • Patient with Acute Ischemic Stroke within 24 hours from symptoms o
  • Age 18-85 years old
  • Consent process is completed per international and local regulations

Age in the registry: 18 years to 85 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
National Institute of Mental Health, Neurology and Neurosurgery)
Coordinator of this site? Confirm its status
BudapestHungaryUnknown status
Shaare Zedek
Coordinator of this site? Confirm its status
JerusalemIsraelUnknown status
Sheba medical center
Coordinator of this site? Confirm its status
Ramat GanIsraelUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.