Loading clinical trials...
Loading clinical trials...
Outcomes of Intra-arterial and Endosaccular Flow Diverters for Treatment of Intracranial Aneurysms - International Registry of Intra-arterial and Endosaccular Flow Diverters (IRF)
This multicenter retrospective cohort study aims to evaluate and compare the technical performance, safety, and clinical outcomes of intracranial aneurysms treated with flow diverter stents and endosaccular flow disruptors.
Flow diverters and endosaccular flow disruptors used for the treatment of intracranial aneurysms exhibit distinct procedural and clinical outcomes, with potential differences in device-specific parameters such as procedure time, radiation exposure, adjunct device requirements, and long-term angiographic success. Since the completion of the Pipeline Embolization Device (PED) for the Intracranial Treatment of Aneurysms trial, the field of flow diversion has undergone continuous evolution with the development and approval of several devices. While these devices share a similar mechanism for aneurysm occlusion, their design and delivery systems can vary significantly. Various studies have demonstrated a promising safety and efficacy profile; however, the available data for a direct comparison of the technical and clinical outcomes between these devices remains limited.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
University of Miami
Coral Gables, Florida, United States
Mayo Clinic Florida
Jacksonville, Florida, United States
Sarasota Memorial Research Institute
Sarasota, Florida, United States
Lahey Hospital and Medical Center
Burlington, Massachusetts, United States
Munson Medical Center
Traverse City, Michigan, United States
Robert Wood Johnson University
New Brunswick, New Jersey, United States
University at Buffalo
Buffalo, New York, United States
Montefiore Medical Center Department of Neurosurgery
The Bronx, New York, United States
Geisinger Health
Danville, Pennsylvania, United States
HCA Houston Healthcare Kingwood
Kingwood, Texas, United States
Start Date
October 1, 2023
Primary Completion Date
June 1, 2026
Completion Date
June 1, 2026
Last Updated
January 7, 2026
5,000
ESTIMATED participants
Lead Sponsor
Montefiore Medical Center
Collaborators
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT04927156