Diagnostic Comparison of PET-magnetic Resonance and PET-CT in Patients With Oncologic Diseases
NCT ID: NCT02316431
Last Updated: 2016-12-16
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
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COMPLETED
142 participants
OBSERVATIONAL
2014-12-31
2016-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Written informed consent
* Patients with a proven or suspected oncological disease referred for a clinically -Indicated PET/CT with of without contrast media
Exclusion Criteria
* Non compliance of the patient to follow the study instructions (e.g. hearing problems, dementia)
* Inclusion in another clinical trial 30 days prior to inclusion
* Age \< 30years
* Contraindication for MRI (cardiac pacemaker, certain metal implants, claustrophobia
* Known allergies to contrast CT or MRI contrast media
* Patients with an glomerular filtration rate of \< 60ml/min/1.73m2
18 Years
90 Years
ALL
No
Sponsors
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University of Zurich
OTHER
Responsible Party
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Principal Investigators
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Patrick Veit-Haibach, MD
Role: PRINCIPAL_INVESTIGATOR
University of Zurich
Locations
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University Hospital Zurich, Diagnostic and Interventional Radiology
Zurich, Canton of Zurich, Switzerland
Countries
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References
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Sekine T, Delso G, Zeimpekis KG, de Galiza Barbosa F, Ter Voert EEGW, Huellner M, Veit-Haibach P. Reduction of 18F-FDG Dose in Clinical PET/MR Imaging by Using Silicon Photomultiplier Detectors. Radiology. 2018 Jan;286(1):249-259. doi: 10.1148/radiol.2017162305. Epub 2017 Sep 14.
Other Identifiers
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KEK-ZH-Nr. 2014-0072
Identifier Type: -
Identifier Source: org_study_id