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Patient Acceptance of Whole Body Magnetic Resonance Angiography

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00556101
First Posted: November 9, 2007
Last Update Posted: August 19, 2009
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
Rigshospitalet, Denmark
Information provided by:
Copenhagen University Hospital at Herlev
  Purpose

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.


Condition Intervention
Atherosclerosis Intermittent Claudication MRI Procedure: Whole body magnetic resonance angiography

Study Type: Observational
Study Design: Time Perspective: Prospective
Official Title: Whole Body Magnetic Resonance Angiography: Questionnaire Examination of Patient Acceptance.

Further study details as provided by Copenhagen University Hospital at Herlev:

Primary Outcome Measures:
  • Patient acceptance of Whole body MRA

Estimated Enrollment: 81
Study Start Date: November 2007
Study Completion Date: July 2009
Detailed Description:

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.

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients with pheripheral arterial disease
Criteria

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
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00556101


Locations
Denmark
Department of Radiology, Herlev University Hospital
Herlev Copenhagen, Herlev, Denmark, DK2730
Sponsors and Collaborators
Copenhagen University Hospital at Herlev
Rigshospitalet, Denmark
Investigators
Study Chair: Henrik S Thomsen, Prof. MD. University Hospital at Herlev Copenhagen Denmark
  More Information

ClinicalTrials.gov Identifier: NCT00556101     History of Changes
Other Study ID Numbers: WB-angio herlev 4
First Submitted: November 8, 2007
First Posted: November 9, 2007
Last Update Posted: August 19, 2009
Last Verified: August 2009

Keywords provided by Copenhagen University Hospital at Herlev:
Magnetic resonance
whole body
angiography
questionnaire

Additional relevant MeSH terms:
Atherosclerosis
Intermittent Claudication
Arteriosclerosis
Arterial Occlusive Diseases
Vascular Diseases
Cardiovascular Diseases
Signs and Symptoms