Inari VISION Registry

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT06600542

Enrollment

1000

Registered

2024-09-19

Start date

2025-03-07

Completion date

2029-12-31

Last updated

2026-08-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pulmonary Embolism

Brief summary

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

Interventions

DEVICEInari Medical Commercially Available Devices

Commercially approved Inari Medical devices

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

1. Willing and able to provide informed consent per institution and geographical requirements 2. 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. 3. Currently within enrollment window relative to their procedure 4. Age ≥ 18 years

Exclusion criteria

1. Is or will be inaccessible for registry follow-up 2. Meets

Design outcomes

Primary

Measure	Time frame
Incidence of device-related, procedure-related, or fatal Adverse Events	Up to 180 days

Countries

Italy, Portugal, United Kingdom

Contacts

CONTACTIda Nelson

ida.nelson@inarimedical.com46 707 723010

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 12, 2026