Inari VISION Registry
Recruiting now
Conditions studied: Pulmonary Embolism
In brief
This registry is a global prospective, non-randomized, multicenter, observational, active post-market data collection of Inari Medical devices and products.
Key facts
- Study ID
- NCT06600542
- Run by
- Inari Medical
- People needed
- 1000
- Starts
- 2025-03-07
- Expected to finish
- 2029-12-31
- Last updated by the study team
- 2026-07-08
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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
You may not qualify if…
- 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
Where it is running
- Azienda Ospedaliero Universitaria delle Marche — Ancona, Italy (enrolling)
- Santa Marta Hospital — Lisbon, Portugal (enrolling)
- Southmead Hospital Bristol — Bristol, United Kingdom (enrolling)
- Queen Elizabeth University Hospital — Glasgow, United Kingdom (enrolling)
- Northwick Park Hospital — London, United Kingdom (enrolling)
- Royal Free Hospital — London, United Kingdom (enrolling)
- Royal London — London, United Kingdom (enrolling)
- UCLH University College London Hospital — London, United Kingdom (enrolling)
- Royal Victoria Infirmary — Newcastle, United Kingdom (enrolling)
- Great Western Hospital — Swindon, United Kingdom (enrolling)
Full record on ClinicalTrials.gov
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