New registry to monitor safety of LOBO device in bleeding emergencies
NCT ID NCT07525518
First seen Jun 27, 2026 · Last updated Jul 22, 2026 · Updated 2 times
Summary
This registry will follow 500 adults who receive the LOBO Vascular Occlusion System, a device used to block blood vessels in cases of arterial bleeding or other conditions. The goal is to see how safe and effective the device is in everyday medical practice. Participants are enrolled after treatment, and the study will track device-related complications and how well the device stops bleeding.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- Active substance
- LOBO Vascular Occlusion System (a device used to block blood vessels)
- What this could lead to
- If successful, this registry will provide real-world data on how well the LOBO device works and its safety, helping doctors make better treatment decisions.
- What could go wrong
- This is an observational registry, not a controlled trial, so it cannot prove cause and effect. Results may be limited by patient selection and lack of a comparison group.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Charlotte Radiology
Charlotte, North Carolina, 28202, United States
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UMASS Chan Medical School
Worcester, Massachusetts, 01655, United States
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University of Colorado
Aurora, Colorado, 80045, United States
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University of North Carolina at Chapel Hill
Chapel Hill, North Carolina, 27599, United States
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