Patient Acceptance of Whole Body Magnetic Resonance Angiography

This study has been completed.
Sponsor:
Collaborator:
Rigshospitalet, Denmark
Information provided by:
Copenhagen University Hospital at Herlev
ClinicalTrials.gov Identifier:
NCT00556101
First received: November 8, 2007
Last updated: August 18, 2009
Last verified: August 2009

November 8, 2007
August 18, 2009
November 2007
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Patient acceptance of Whole body MRA
Same as current
Complete list of historical versions of study NCT00556101 on ClinicalTrials.gov Archive Site
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Patient Acceptance of Whole Body Magnetic Resonance Angiography
Whole Body Magnetic Resonance Angiography: Questionnaire Examination of Patient Acceptance.

Investigation of how the patients experience whole body MRA. After the WB-MRA the patients will fill in a questionnaire, that contains questions about the WB-MRA procedure and how the patient felt during the examination.

We expect that the patients will report a high degree of satisfaction with the WB-MRA procedure, with little discomfort.

WB-MRA is performed in patients referred for conventional x-ray based angiography. The WB-MRA is performed first in all patients.

After both examinations are completed the patients will be asked to fill in a questionnaire containing questions about their experience of the 2 procedures.

We will then compare the results for the procedures.

Observational
Time Perspective: Prospective
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Non-Probability Sample

Patients with pheripheral arterial disease

  • Atherosclerosis
  • Intermittent Claudication
  • MRI
Procedure: Whole body magnetic resonance angiography
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
81
July 2009
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Inclusion Criteria:

  • Symptomatic lower extremity ischemia (claudication, ischemic wounds)
  • Referred to digital subtraction angiography (DSA)

Exclusion Criteria:

  • Renal insufficiency (GFR < 30 ml/min)
  • Contra-indications for MRI-examination (claustrophobia, metal-implants, pacemaker)
  • Dementia
  • Pregnancy/lactation
  • Allergy to gadolinium based MRI contrast agents
  • Acute disease
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
Denmark
 
NCT00556101
WB-angio herlev 4
Yes
Not Provided
Copenhagen University Hospital at Herlev
Rigshospitalet, Denmark
Study Chair: Henrik S Thomsen, Prof. MD. University Hospital at Herlev Copenhagen Denmark
Copenhagen University Hospital at Herlev
August 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP