Viewing Study NCT02295137



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Study NCT ID: NCT02295137
Status: UNKNOWN
Last Update Posted: 2014-11-20
First Post: 2014-10-27

Brief Title: Image Fusion of Preprocedural CTA With Real Time Fluoroscopy to Enhance EVAR Repair
Sponsor: University Health Network Toronto
Organization: University Health Network Toronto

Study Overview

Official Title: Image Fusion of Pre-procedural CTA With Real-time Fluoroscopy to Guide Proper Renal and Visceral Arteries Catheterization During Advanced Endovascular Aortic Aneurysms Repair A Feasibility Study
Status: UNKNOWN
Status Verified Date: 2014-10
Last Known Status: RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Abdominal Aortic Aneurysm AAA is a potentially life threatening condition If the aneurysm ruptures the mortality can be as high as 80 Endovascular aneurysms repair EVAR is a minimal invasive procedure and has been widely used on treating AAA Advanced endovascular techniques are used to treat patients with more complex pathology by using custom-made devices and additional stents In order to accomplish the technical success on advanced EVAR with the current imaging equipment and technique for EVAR procedures ie live x-ray fluoroscopy and 2-D digital subtraction angiography DSA multiple angiograms on the target arteries arteriograms are required Subsequently patients are exposed to higher dose of contrast and radiation compared to conventional EVAR This study is to assess the feasibility of proper visceral and renal arteries catheterization using a 3D model obtained from pre-procedural computed tomographic angiography CTA fused with real-time fluoroscopy without contrast injection or angiographic run-offs thus minimizing the contrast use and patient radiation exposure while achieving procedure success during Advanced EVAR
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None