Inari VISION Registry

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

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Key information

Conditions

Pulmonary Embolism Cardiovascular Diseases Embolism Embolism and Thrombosis Lung Diseases Respiratory Tract Diseases Vascular Diseases

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Azienda Ospedaliero Universitaria delle Marche, Ancona, Italy

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Willing and able to provide informed consent per institution and geographical requirements
Has received treatment with an eligible Inari Medical device. NOTE: If patients are consented prior to their procedure and the procedure does not take place, the patient will be considered a screen failure.
Currently within enrollment window relative to their procedure
Age ≥ 18 years

Exclusion criteria

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, in the investigator's opinion, would interfere with participation in this registry
Is pregnant or breastfeeding at the time of enrollment

Treatment and study plan

Inari Medical Commercially Available Devices

Device

Commercially approved Inari Medical devices

Primary outcomes

Incidence of device-related, procedure-related, or fatal Adverse Events

Time frame: Up to 180 days

Study contacts

Contact information is provided by the study sponsor or research team.

Ida Nelson

CONTACT

[email protected]

46 707 723010

Sponsors and collaborators

Lead sponsor

Inari Medical

Industry

Registry information

Important dates

Study start: 2025
Primary completion: 2029
Study completion: 2029
First posted: Sep 19, 2024
Registry last updated: Jul 8, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

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