DynaCT Imaging in EVAR: Comparing Clinical Benefit of DynaCT to Multidetector CT as the Current Gold Standard.
Use of DynaCT in Endovascular Treatment of Abdominal Aortic Aneurysm. Evaluation of Image Quality.
1 other identifier
interventional
20
1 country
1
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Dec 2005
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 1, 2005
CompletedFirst Submitted
Initial submission to the registry
December 12, 2005
CompletedFirst Posted
Study publicly available on registry
December 13, 2005
CompletedStudy Completion
Last participant's last visit for all outcomes
March 1, 2007
CompletedFebruary 28, 2014
February 1, 2014
December 12, 2005
February 27, 2014
Conditions
Outcome Measures
Primary Outcomes (1)
Evidence og clinical benefit of new imaging functionality.
3 days (pluss or minus 3 days).
Interventions
Eligibility Criteria
You may qualify if:
- Age over 65,
- Satisfactory renal function
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Norwegian University of Science and Technologylead
- St. Olavs Hospitalcollaborator
Study Sites (1)
St. Olavs Hosptial
Trondheim, 7006, Norway
Related Publications (1)
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.
PMID: 19010697RESULT
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Kari R Eide, MS
NTNU/St.Olavs Hospital
- STUDY CHAIR
Olav Haraldseth, PhD MD
National Taiwan Normal University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- DIAGNOSTIC
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 12, 2005
First Posted
December 13, 2005
Study Start
December 1, 2005
Study Completion
March 1, 2007
Last Updated
February 28, 2014
Record last verified: 2014-02