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NCT06170619: OCCLUDE

Obsidio™ Conformable Embolic Registry

Completed Last updated 17 March 2026
What this trial tests

trial testing Obsidio™ Conformable Embolic in Hypervascular Tumors in 125 participants. Completed in 9 September 2025.

Timeline
19 June 2024
Primary endpoint
9 September 2025
9 September 2025

Quick facts

Lead sponsorBoston Scientific Corporation
StatusCompleted
Study typeOBSERVATIONAL
Enrollment125
Start date19 June 2024
Primary completion9 September 2025
Estimated completion9 September 2025
Sites20 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Boston Scientific Corporation — full company profile →

Who can join

18 and older, any sex, with Hypervascular Tumors or Bleeding. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Boston Scientific Corporation trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06170619.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing