DynaCT Imaging in EVAR: Comparing Clinical Benefit of DynaCT to Multidetector CT as the Current Gold Standard.
Primary Purpose
Abdominal Aortic Aneurysm
Status
Completed
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
DynaCT
Sponsored by
About this trial
This is an interventional diagnostic trial for Abdominal Aortic Aneurysm
Eligibility Criteria
Inclusion Criteria: Age over 65, Satisfactory renal function
Sites / Locations
- St. Olavs Hosptial
Outcomes
Primary Outcome Measures
Evidence og clinical benefit of new imaging functionality.
Secondary Outcome Measures
Full Information
NCT ID
NCT00264862
First Posted
December 12, 2005
Last Updated
February 27, 2014
Sponsor
Norwegian University of Science and Technology
Collaborators
St. Olavs Hospital
1. Study Identification
Unique Protocol Identification Number
NCT00264862
Brief Title
DynaCT Imaging in EVAR: Comparing Clinical Benefit of DynaCT to Multidetector CT as the Current Gold Standard.
Official Title
Use of DynaCT in Endovascular Treatment of Abdominal Aortic Aneurysm. Evaluation of Image Quality.
Study Type
Interventional
2. Study Status
Record Verification Date
February 2014
Overall Recruitment Status
Completed
Study Start Date
December 2005 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
March 2007 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Norwegian University of Science and Technology
Collaborators
St. Olavs Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The aim of this study is to evaluate a new way to create CT-like images during intra-operative procedures. We want to prove that the quality and information received from DynaCT is satisfactory in implementing stent-graft in abdominal aortic aneurysm.
Detailed Description
The study will compare images from the new modality (DynaCT) with the present modality (Multi detectorCT). We make three different set of images from each modality.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Abdominal Aortic Aneurysm
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
20 (Actual)
8. Arms, Groups, and Interventions
Intervention Type
Procedure
Intervention Name(s)
DynaCT
Primary Outcome Measure Information:
Title
Evidence og clinical benefit of new imaging functionality.
Time Frame
3 days (pluss or minus 3 days).
10. Eligibility
Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age over 65,
Satisfactory renal function
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kari R Eide, MS
Organizational Affiliation
NTNU/St.Olavs Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Olav Haraldseth, PhD MD
Organizational Affiliation
National Taiwan Normal University
Official's Role
Study Chair
Facility Information:
Facility Name
St. Olavs Hosptial
City
Trondheim
ZIP/Postal Code
7006
Country
Norway
12. IPD Sharing Statement
Citations:
PubMed Identifier
19010697
Citation
Eide KR, Odegard A, Myhre HO, Lydersen S, Hatlinghus S, Haraldseth O. DynaCT during EVAR--a comparison with multidetector CT. Eur J Vasc Endovasc Surg. 2009 Jan;37(1):23-30. doi: 10.1016/j.ejvs.2008.09.017. Epub 2008 Nov 17.
Results Reference
result
Learn more about this trial
DynaCT Imaging in EVAR: Comparing Clinical Benefit of DynaCT to Multidetector CT as the Current Gold Standard.
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