ClinicaliQ Trial Snapshot
- Inari VISION Registry — Recruiting • Cardiology / Cardiovascular • NCT06600542.
- What is being tested: The Inari VISION Registry collects real-world performance data on Inari Medical devices and products through prospective, multicenter observation without randomization, enabling assessment of safety and efficacy across diverse clinical settings.
- Patient eligibility overview: This is a global observational registry enrolling patients receiving Inari Medical interventions across multiple centers; specific inclusion criteria are determined by the clinical indication for each device rather than a single standardized patient population.
Use This Page For
- Quick orientation before opening the registry record.
- Checking recruitment status, phase and sponsor at a glance.
- Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying
This registry is a global prospective, non-randomized, multicenter, observational, active post-market data collection of Inari Medical devices and products.
Eligibility Snapshot
- : 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
Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.