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Flow Arrest Safety and Technical Success With Balloon Guide Catheters

NCT04416659 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 52

Last updated 2022-04-28

No results posted yet for this study

Summary

The objective of this post-market registry is to assess technical efficacy and safety associated with the use of the BOSS Balloon Guide Catheter during neuro-vascular procedures while providing temporary arrest of blood flow.

Conditions

  • Acute Ischemic Stroke

Interventions

DEVICE

Neuro-vascular access

Adjunctive device providing a conduit for retrieval device during thrombectomy

Sponsors & Collaborators

  • Medtronic Neurovascular Clinical Affairs

    lead INDUSTRY

Principal Investigators

  • Biraj Patel, MD · Carilion Clinic

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-01-12
Primary Completion
2021-10-27
Completion
2021-10-27

Countries

  • United States

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 NCT04416659 on ClinicalTrials.gov