DynaCT Imaging in EVAR: Comparing Clinical Benefit of DynaCT to Multidetector CT as the Current Gold Standard.

Sponsor
Norwegian University of Science and Technology (Other)
Overall Status
Completed
CT.gov ID
NCT00264862
Collaborator
St. Olavs Hospital (Other)
20
1
14.9
1.3

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Procedure: DynaCT
N/A

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
20 participants
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Use of DynaCT in Endovascular Treatment of Abdominal Aortic Aneurysm. Evaluation of Image Quality.
Study Start Date :
Dec 1, 2005
Actual Study Completion Date :
Mar 1, 2007

Outcome Measures

Primary Outcome Measures

  1. Evidence og clinical benefit of new imaging functionality. [3 days (pluss or minus 3 days).]

Eligibility Criteria

Criteria

Ages Eligible for Study:
65 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age over 65,

  • Satisfactory renal function

Contacts and Locations

Locations

Site City State Country Postal Code
1 St. Olavs Hosptial Trondheim Norway 7006

Sponsors and Collaborators

  • Norwegian University of Science and Technology
  • St. Olavs Hospital

Investigators

  • Principal Investigator: Kari R Eide, MS, NTNU/St.Olavs Hospital
  • Study Chair: Olav Haraldseth, PhD MD, National Taiwan Normal University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Norwegian University of Science and Technology
ClinicalTrials.gov Identifier:
NCT00264862
Other Study ID Numbers:
  • FOR2008_1
First Posted:
Dec 13, 2005
Last Update Posted:
Feb 28, 2014
Last Verified:
Feb 1, 2014
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 28, 2014