Inari VISION Registry

Launched by INARI MEDICAL · Sep 16, 2024

Keywords

ClinConnect Summary

The Inari VISION Registry is a study that aims to collect information about devices and products made by Inari Medical, which are used to treat a condition called pulmonary embolism (a blockage in the lungs' blood vessels). This registry is open to patients worldwide who have received treatment with these devices. The study is currently recruiting participants who are at least 18 years old and can provide consent to take part in the registry. To join, patients must have already had treatment with an Inari Medical device and be within the enrollment period around their procedure.

Participants in this registry can expect to share their experiences and health outcomes after using the Inari devices. It’s important to know that people who are pregnant, breastfeeding, or involved in other studies that might interfere with this one cannot participate. The goal of this registry is to gather important data to help understand how well these devices work and to improve future treatments for pulmonary embolism.

Gender

ALL

Eligibility criteria

• 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 exclusion criteria required by local requirements
• • 3. Current or planned participation in another drug or device study that, in the investigator's opinion, would interfere with participation in this registry
• • 4. Is pregnant or breastfeeding at the time of enrollment