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Clinical trialNCT04518670CompletedObservational

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

SponsorRapid MedicalEnrollment90Intracranial Aneurysm
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

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.
clinicaltrials.gov ↗

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

8 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Usa Health University Hospital

    Mobile, Alabama, United States

  • Carondelet St. Joseph'S Hospital (tenet)

    Tucson, Arizona, United States

  • Santa Barbara Cottage

    Santa Barbara, California, United States

  • Los Robles

    Thousand Oaks, California, United States

  • Baptist Health Research Institute

    Jacksonville, Florida, United States

  • St. Mary'S Medical Ctr (tenet)

    West Palm Beach, Florida, United States

  • University of Buffalo

    Buffalo, New York, United States

  • Texas Stroke Institute (sarah Cannon Tn)

    Dallas, Texas, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
24 Nov 2020
Primary completion
1 May 2024
Completion
7 Jul 2024
Last update posted
21 Jan 2026
Registered enrollment
90
Registry id
NCT04518670
clinicaltrials.gov ↗

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.