Inari VISION Registry
ConditionPulmonary Embolism
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorInari Medical
About this trial
This registry is a global prospective, non-randomized, multicenter, observational, active post-market data collection of Inari Medical devices and products.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
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
Disqualifiers
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
Trial population
Patients who have been treated with an Inari Medical device.
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Inari Medical Commercially Available Devices
DeviceCommercially approved Inari Medical devices
Treatment groups
No treatment groups listed
Trial outcomes
Primary outcomes
1
Incidence of device-related, procedure-related, or fatal Adverse Events
Time frame
Up to 180 daysSponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov