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Obsidio™ Conformable Embolic Registry

Completed · NCT06170619

Conditions: Hypervascular Tumors, Bleeding, Hemorrhage

At a glance

Research payments reported, 2025
$621,856
U.S. investigators named
20
Sites paid
20
Planned or actual enrollment
125

About the trial

Sponsor
Boston Scientific Corporation
Tested
Obsidio™ Conformable Embolic (device)
Dates
Started 2024-06-19; completion 2025-09-09
Results posted
Not yet

OCCLUDE is a prospective, post-approval, open-label, single arm, multi-center US registry of patients who undergo embolization with Obsidio™ Conformable Embolic. The purpose of this Registry is to assess effectiveness and safety outcomes of subjects who undergo embolization with Obsidio.

From ClinicalTrials.gov, last updated 2026-06-01. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Boston Scientific Corporation reported $621,856 in research payments for this study in 2025 (130 payments).

Products named: Clinical Trial Product

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

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