Actively Recruiting

Age: 18Years +
All Genders
NCT06600542

Inari VISION Registry

Led by Inari Medical · Updated on 2026-05-05

1000

Participants Needed

10

Research Sites

251 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This registry is a global prospective, non-randomized, multicenter, observational, active post-market data collection of Inari Medical devices and products.

CONDITIONS

Official Title

Inari VISION Registry

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Willing and able to provide informed consent per institution and geographical requirements
  • Has received treatment with an eligible Inari Medical device
  • Currently within enrollment window relative to their procedure
  • Age 18 years or older
Not Eligible

You will not qualify if you...

  • Is or will be inaccessible for registry follow-up
  • Meets exclusion criteria required by local requirements
  • Current or planned participation in another drug or device study that would interfere with participation
  • Is pregnant or breastfeeding at the time of enrollment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 10 locations

1

Azienda Ospedaliero Universitaria delle Marche

Ancona, Italy

Actively Recruiting

2

Santa Marta Hospital

Lisbon, Portugal

Actively Recruiting

3

Southmead Hospital Bristol

Bristol, United Kingdom

Actively Recruiting

4

Queen Elizabeth University Hospital

Glasgow, United Kingdom

Actively Recruiting

5

Northwick Park Hospital

London, United Kingdom

Actively Recruiting

6

Royal Free Hospital

London, United Kingdom

Actively Recruiting

7

Royal London

London, United Kingdom

Actively Recruiting

8

UCLH University College London Hospital

London, United Kingdom

Actively Recruiting

9

Royal Victoria Infirmary

Newcastle, United Kingdom

Actively Recruiting

10

Great Western Hospital

Swindon, United Kingdom

Actively Recruiting

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Research Team

I

Ida Nelson

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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