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Completed No phase listed Observational Results available

Success in Comaneci-assist Coils Embolization Surveillance Study (SUCCESS)

ClinicalTrials.gov ID: NCT04518670

Public ClinicalTrials.gov record NCT04518670. 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 Nov 10, 2026, 8:12 PM EST

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Official title

Success in Comaneci-assist Coils Embolization Surveillance Study

Brief summary

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

The Comaneci Embolization Assist Device is indicated for use in the neurovasculature as a temporary endovascular device used to assist in the coil embolization of wide-necked intracranial aneurysms with a neck width ≤ 10 mm. A wide-necked intracranial aneurysm (IA) defines the neck width as ≥ 4 mm or a dome-to-neck ratio \< 2. The objective of the Postmarket Surveillance Plan is to assess safety and performance as used in postmarket clinical practice in the U.S.

Study identification

NCT ID
NCT04518670
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Rapid Medical
Industry
Enrollment
90 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 85 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
Nov 24, 2020 (Actual)
Primary completion
May 1, 2024 (Actual)
Completion
Jul 7, 2024 (Actual)
Last update posted
Jan 21, 2026

2020 – 2024

United States locations

U.S. sites
8
U.S. states
6
U.S. cities
8
Facility City State ZIP Site status
USA Health University Hospital Mobile Alabama 36617 —
Carondelet St. Joseph's Hospital (Tenet) Tucson Arizona 85711 —
Santa Barbara Cottage Santa Barbara California 93105 —
Los Robles Thousand Oaks California 91360 —
Baptist Health Research Institute Jacksonville Florida 32207 —
St. Mary's Medical Ctr (Tenet) West Palm Beach Florida 33407 —
University of Buffalo Buffalo New York 14203 —
Texas Stroke Institute (Sarah Cannon TN) Dallas Texas 75075 —

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 NCT04518670, 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 Jan 21, 2026 · Synced Nov 10, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04518670 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →