Recruiting NCT06600542
Inari VISION Registry
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Inari Medical Commercially Available Devices.
- Who it may be relevant to
- Registry conditions: Pulmonary Embolism. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Italy, Portugal, United Kingdom
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
This registry is a global prospective, non-randomized, multicenter, observational, active post-market data collection of Inari Medical devices and products.
Interventions
- Device Inari Medical Commercially Available Devices
Commercially approved Inari Medical devices
Primary outcome measures
- Incidence of device-related, procedure-related, or fatal Adverse Events [Time frame: Up to 180 days]
Eligibility criteria
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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
United Kingdom · 8 centers
- Southmead Hospital Bristol — Bristol
- Queen Elizabeth University Hospital — Glasgow
- Northwick Park Hospital — London
- Royal Free Hospital — London
- Royal London — London
- UCLH University College London Hospital — London
- Royal Victoria Infirmary — Newcastle
- Great Western Hospital — Swindon
Italy · 1 center
- Azienda Ospedaliero Universitaria delle Marche — Ancona
Portugal · 1 center
- Santa Marta Hospital — Lisbon
Identifiers
NCT: NCT06600542 · 24-003