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Magnetic Resonance Imaging clinical trials

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NCT ID: NCT03224975 Terminated - Clinical trials for Magnetic Resonance Imaging

Acute Pain Memory Among Former Burned: Exploration of fMRI.

EXPLO-DMA
Start date: February 13, 2018
Phase: N/A
Study type: Interventional

Pain is complex phenomenon misunderstood in spite of medical progress and neurosciences. That's why the relief of chronic pain is only partial for a lot of infection as arthrosis, chronic back pain, headaches or neuropathic pain. Certain situations bring to relive pain sensation. Investigators were interested to former burned. They wonder about somatic memory and unconscious of acute.

NCT ID: NCT02195024 Terminated - Clinical trials for Magnetic Resonance Imaging

Cardiac MRI After Pacemaker Replacement

MRI-rePACE
Start date: July 2014
Phase: Phase 4
Study type: Interventional

Aim of this trial is to investigate feasibility of cardiac magnetic resonance imaging (cMRI) in patients with long term implanted coradial leads upgraded to an MRI conditional pacemaker system, to assess MR-image quality and to prove the safety of MRI in this specific population in the short term as well as during long term follow-up.

NCT ID: NCT02084628 Terminated - Clinical trials for Magnetic Resonance Imaging

Magnetic Resonance Imaging of the Liver in Children 0-2 Months of Age With an Intravenous Injection of Eovist/Primovist Which is a Contrast Agent

Start date: February 2015
Phase: Phase 3
Study type: Interventional

This is an open-label, multi-center study involving babies 0-2 months of age who have liver problems (pathology) and need to have their liver and possibly, the bile ducts imaged using magnetic resonance imaging and injection of a contrast agent (dye). This agent is called Eovist. It has been marketed since 2004 and used in many countries all over the world. The baby will have blood tests before and after the imaging is done to make sure that there are no unexpected findings before and after the imaging. Also 3 blood samples up to 8 hours after the injection will be obtained in order to measure how much of the dye is in the blood. The baby will have an intravenous line which can be used for the blood samples and will not need to be stick for the blood samples. Several radiologists will evaluate the images. The family doctor will be contacted to find out what was the diagnosis and treatment after the results of the MRI were known. Six months after the study, the parent(s)/legal guardian(s) will be contacted to make sure the that baby did not have any problems, especially with the skin, joints and eyes.

NCT ID: NCT00894751 Terminated - Anesthesia Clinical Trials

Two Anesthetic Techniques in Magnetic Resonance Imaging (MRI)

Start date: January 2009
Phase: Phase 1
Study type: Interventional

The goal of this study is to determine if there is a significant difference in the quality of care between the investigators' two standard anesthesia techniques for children undergoing a MRI of the body and/or extremity MRI. Quality of care will be measured by time spent in the MRI room as well as parental satisfaction, frequency of interruptions of the MRI scan, incidence-severity of respiratory complications, post anesthesia agitation, and time spent in the induction room, MRI room, and Post-Anesthesia Care Unit (PACU).