New Stent Retriever, VERSI System for AIS

NCT03366818 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2019-10-15

No results posted yet for this study

Summary

To confirm efficacy and safety of VERSI system for acute ischemic stroke

Conditions

  • Acute Ischemic Stroke

Interventions

DEVICE

thrombectomy

mechanical thrombectomy

Sponsors & Collaborators

  • Kobe City General Hospital

    lead OTHER

Principal Investigators

  • Nobuyuki Sakai, MD DMSc · Kobe City Medical Center General Hospital, Kobe, Japan

Study Design

Allocation
NA
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-09-21
Primary Completion
2018-03-31
Completion
2019-03-31

Countries

  • Japan

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 NCT03366818 on ClinicalTrials.gov