The Vesalio NeVa Stent Retriever Study for Treatment of Large Vessel Occlusion Strokes

NCT03927001 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 150

Last updated 2023-01-17

No results posted yet for this study

Summary

A prospective, open label, single-arm 90-day 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 Retrievers

mechanical neurothrombectomy

Sponsors & Collaborators

  • Vesalio

    lead INDUSTRY

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
2019-04-01
Primary Completion
2024-08-31
Completion
2024-08-31
FDA Device
Yes

Countries

  • Spain

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 NCT03927001 on ClinicalTrials.gov