ClotTriever® Thrombectomy System Use-Result Survey in Japan

Inari Medical

Status: Invitation-only

Conditions: Deep Vein Thrombosis

Treatments: Device: ClotTriever® Thrombectomy System

Study type: Observational

Funder types: Industry; Other

Identifiers

NCT06871683

24-001

Details and patient eligibility

About

The objective of this survey is to determine the safety and efficacy of the ClotTriever Thrombectomy System under daily clinical practice after marketing approval in Japan.

This device was designated as a subject of use results evaluation at the time of application for manufacturing and marketing approval.

Enrollment: 100 estimated patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

This is an all-comers survey of all patients treated with ClotTriever® Thrombectomy System in Japan.

Trial design

100 participants in 1 patient group

Full Analysis Population

Description:

All subjects who the survey device entered their vasculature.

Treatment:

Device: ClotTriever® Thrombectomy System