Actively Recruiting

Age: 18Years - 75Years
All Genders
NCT05531461

Cognition and Imaging With Tigertriever

Led by Rapid Medical · Updated on 2025-05-16

424

Participants Needed

3

Research Sites

104 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The objective of the COGNITIVE Study is to evaluate whether successful reperfusion with Tigertriever is associated with cognitive benefit.

CONDITIONS

Official Title

Cognition and Imaging With Tigertriever

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients admitted with large vessel occlusion (LVO) and treated with the Tigertriever, as indicated per the approved IFU.
  • Tigertriever was used as the first line treatment in the target vessel.
  • A signed informed consent.
  • Age 18-75 years (inclusive).
  • No known significant pre-stroke disability (pre-stroke mRS 0 or 1).
Not Eligible

You will not qualify if you...

  • Use of any other IA recanalization device prior to the Tigertriever in the target vessel, including aspiration catheter.
  • Evidence of acute brain hemorrhage on CT and/or MRI at admission.
  • Prior hemorrhage, stroke, thrombolysis, and/or endovascular therapy in the last 3 months.
  • Probable cerebral amyloid angiopathy.
  • Pre-stroke diagnosed dementia and/or prescribed cholinesterase inhibitors.
  • Pre-stroke diagnosed and/or currently treated major depression.
  • Pre-stroke learning or intellectual disability.
  • Anticipated inability to obtain 6-month follow-up assessments.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 3 locations

1

University of California

Los Angeles, California, United States, 90095

Actively Recruiting

2

Corewell Health Research Institute

Grand Rapids, Michigan, United States, 49503

Actively Recruiting

3

Westchester Medical Center

New York, New York, United States, 10595

Actively Recruiting

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Research Team

W

Walid Haddad, Dr.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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