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Efficacy & Safety of LOBO™ Vascular Occlusion Device for Embolization of Pulmonary Arteriovenous Malformations

Active, not recruiting · Not applicable · NCT06735976

Conditions: Pulmonary Arteriovenous Malformations

At a glance

Research payments reported, 2025
$40,000
U.S. investigators named
1
Sites paid
1
Planned or actual enrollment
30

About the trial

Sponsor
University of North Carolina, Chapel Hill (with Okami Medical, Inc.)
Tested
PAVM Embolization (device), PAVM Embolization with a LOBO™ device (device)
Dates
Started 2024-12-17; completion 2029-05
Results posted
Not yet

The goal of this clinical trial is to evaluate both the technical success and efficacy of using the LOBO™ device in patients undergoing embolization of Pulmonary Arteriovenous Malformations (PAVM). The main question\[s\] it aims to answer \[is/are\]: * What is the technical success rate, the number of LOBO™ devices needed for occlusion, and time to occlusion for each feeding artery during PAVM embolization using the LOBO™ device? * What is the short-term occlusion rate of the LOBO™ device for PAVM embolization (6 months post-embolization)? * What are the medium- and long-term occlusion rate of the LOBO™ device in PAVMs (12 months and 36 months post embolization)? Researchers will compare …

From ClinicalTrials.gov, last updated 2026-11-06. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Okami Medical, Inc. reported $40,000 in research payments for this study in 2025 (2 payments).

Products named: Lobo

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

  • Unc Chapel Hill School of Medicine $40,000

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.