NCT07525518

Okami Medical ALPHA Registry

Enrolling by Invitation
Not specifiedAges 18+Observational
Okami Medical, Inc.
~500 participants
Updated 2026-07-21 on ClinicalTrials.gov
What's tested:LOBO Vascular Occlusion System

At a glance

Recruiting sites
0 of 4 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Safety Endpoint
Measured over 30 days post-index procedure
+1 more outcome measured
Arterial Bleed
Pulmonary Arteriovenous Malformation
Embolization
Hemorrhage
4 sites across 3 states
North Carolina2
Colorado1
Massachusetts1

This trial hasn't published a contact. View it on ClinicalTrials.gov

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Eligibility criteria

Inclusion

The patient or their legally authorized representative is willing and able to provide informed consent per local requirements
Has or will receive treatment with an eligible Okami Medical device
Age ≥ 18 years

Exclusion

Is or will be inaccessible for registry follow-up
Current or planned participation in a drug or device study that would interfere with participation in this registry or confound the results of this registry in the opinion of the investigator
  • Safety Endpoint30 days post-index procedure

    Incidence of device-related serious adverse events during the index procedure

  • Effectiveness EndpointDuring index procedure

    Technical success of the LOBO Vascular Occlusion System defined as occlusion of the intended target(s) with the LOBO occluder, assessed by angiography