Patient Acceptance of Whole Body Magnetic Resonance Angiography
NCT ID: NCT00556101
Last Updated: 2009-08-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
81 participants
OBSERVATIONAL
2007-11-30
2009-07-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
We expect that the patients will report a high degree of satisfaction with the WB-MRA procedure, with little discomfort.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Whole Body Magnetic Resonance Angiography in Ischemic Patients
NCT00538408
Whole-Body MRA at 3T - A Comparison Between Two Different Scan Protocols
NCT00834548
Whole Body Magnetic Resonance Angiography in Ischemic Patients at 1.5 and 3T
NCT00554073
Technical Development of Cardiovascular Magnetic Resonance Imaging
NCT00027170
Chronic Total Occlusive Lesions CMR Study
NCT05614180
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
PROSPECTIVE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Whole body magnetic resonance angiography
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Referred to digital subtraction angiography (DSA)
Exclusion Criteria
* Contra-indications for MRI-examination (claustrophobia, metal-implants, pacemaker)
* Dementia
* Pregnancy/lactation
* Allergy to gadolinium based MRI contrast agents
* Acute disease
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Rigshospitalet, Denmark
OTHER
Copenhagen University Hospital at Herlev
OTHER
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Henrik S Thomsen, Prof. MD.
Role: STUDY_CHAIR
University Hospital at Herlev Copenhagen Denmark
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Department of Radiology, Herlev University Hospital
Herlev Copenhagen, Herlev, Denmark
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
WB-angio herlev 4
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.