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COMPLETED

Obsidio™ Conformable Embolic Registry

NCT06170619 · View on ClinicalTrials.gov ↗

Study Summary

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.

Interventions

  • DEVICE Obsidio™ Conformable Embolic

Study Locations (20)

California

  • Ronald Reagan UCLA Medical Center — Los Angeles
  • St. Joseph's Medical Center — Stockton

Illinois

  • Northwestern Memorial Hospital — Chicago
  • University of Chicago Hospital — Chicago

Massachusetts

  • Massachusetts General Hospital — Boston
  • Beth Israel Deaconess Medical Center — Boston

New York

  • Albany Medical Center — Albany
  • Mount Sinai Medical Center — New York

Texas

  • The University of Texas MD Anderson Cancer Center — Houston
  • University of Texas Houston Health Science Center — Houston

Arizona

  • Mayo Clinic Hospital — Phoenix

Delaware

  • Christiana Hospital — Newark

District of Columbia

  • MedStar Georgetown University Hospital — Washington D.C.

Trial Details

FieldValue
Enrollment Target 125 participants
Start Date 2024-06-19
Est. Completion 2025-09-09

Sponsor

Boston Scientific Corporation

120 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06170619

The ClinicalTrials.gov registry entry for NCT06170619 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 125 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Boston Scientific Corporation, which has 120 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Bleeding appearing as the primary indexed condition, and to 1 intervention — of which Obsidio™ Conformable Embolic is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06170619 reports 20 study locations spanning 15 distinct geographic areas — top geographies include California, Illinois, Massachusetts. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06170619 about?

NCT06170619 is a clinical study titled "Obsidio™ Conformable Embolic Registry". 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.

What is the current status of trial NCT06170619?

This trial is currently completed. The enrollment target is 125 participants. The study started on 2024-06-19. Estimated completion is 2025-09-09.

What conditions does trial NCT06170619 study?

This clinical trial studies the following conditions: Bleeding, Hemorrhage, Hypervascular Tumors. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06170619?

The interventions under investigation include: Obsidio™ Conformable Embolic (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06170619?

This trial is sponsored by Boston Scientific Corporation, which has 120 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06170619 being conducted?

This trial has 20 study locations across Arizona, California, Delaware, District of Columbia, Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial