NeVa ONE Registry Study

NCT04562194 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 600

Last updated 2026-03-31

No results posted yet for this study

Summary

A prospective, open label study designed to assess the safety, performance and efficacy of thrombus removal in subjects presenting with acute ischemic stroke with the NeVa stent retrievers.

Conditions

  • Acute Ischemic Stroke

Interventions

DEVICE

NeVa Stent Retriever

mechanical neurothrombectomy

Sponsors & Collaborators

  • Vesalio

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-07-01
Primary Completion
2026-12-31
Completion
2027-06-01
FDA Device
Yes

Countries

  • Argentina
  • Italy
  • United Arab Emirates

Study Locations

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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 NCT04562194 on ClinicalTrials.gov