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Active, not recruiting Not applicable Interventional

Citadel Embolization Device Study

ClinicalTrials.gov ID: NCT04057352

Public ClinicalTrials.gov record NCT04057352. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 23, 2026, 5:50 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

The Citadel Embolization Device Study

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to gather safety and effectiveness data on Stryker Neurovascular's Next Generation Target Detachable Coil (hereafter referred to as the Citadel Embolization Device), when used with Target Detachable Coils, in the treatment of wide-neck intracranial aneurysms.

Study identification

NCT ID
NCT04057352
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Not applicable
Lead sponsor
Stryker Neurovascular
Industry
Enrollment
150 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 80 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 17, 2019
Primary completion
Nov 14, 2026
Completion
Nov 14, 2026
Last update posted
Mar 29, 2026

2019 – 2026

United States locations

U.S. sites
25
U.S. states
15
U.S. cities
21
Facility City State ZIP Site status
Cedars-Sinai Medical Center Los Angeles California 90048
California Pacific Medical Center San Francisco California 94114
UCSF Medical Center San Francisco California 94143
John Muir Health Walnut Creek California 94598
RIA Neurovascular Englewood Colorado 80113
University of Florida Gainesville Florida 32608
Baptist Health Jacksonville Florida 32207
University of Miami/Jackson Memorial Miami Florida 33136
Tampa General Hospital Tampa Florida 33606
Northwestern University Chicago Illinois 60611
Indiana Methodist Indianapolis Indiana 46202
Kansas University Medical Center Kansas City Kansas 66160
Baptist Health Lexington Kentucky 40503
University of Kentucky Lexington Kentucky 40506
UMass Memorial Health Worcester Massachusetts 01605
McLaren Health Center Flint Michigan 48532
Spectrum Health Grand Rapids Michigan 49503
Washington University St Louis Missouri 63110
Weill Cornell New York New York 10021
Montefiore Medical Center New York New York 10467
Cleveland Clinic Cleveland Ohio 44195
University of Pennsylvania Hospital Philadelphia Pennsylvania 19104
Thomas Jefferson University Philadelphia Pennsylvania 19107
University of Washington Seattle Washington 98104
West Virginia University Hospital Morgantown West Virginia 26506

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04057352, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 29, 2026 · Synced Sep 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04057352 live on ClinicalTrials.gov.

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