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Clinical trial

Master Study for the MRI Compatibility of the Solia S and Solia T Pacing Lead, the Linoxsmart ProMRI and Linoxsmart ProMRI DF4 ICD (Implantable Cardioverter-defibrillator) Lead and the Corox ProMRI OTW Coronary Sinus Lead in Combination With the Ilesto/Iforia ICD or the Evia/Entovis Triple Chamber Pacemaker

NCT01809665 is registered in ClinicalTrials.gov with Biotronik SE & Co. KG as lead sponsor.

NCT NCT01809665
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Registry record

As filed in ClinicalTrials.gov.

Title
Master Study for the MRI Compatibility of the Solia S and Solia T Pacing Lead, the Linoxsmart ProMRI and Linoxsmart ProMRI DF4 ICD (Implantable Cardioverter-defibrillator) Lead and the Corox ProMRI OTW Coronary Sinus Lead in Combination With the Ilesto/Iforia ICD or the Evia/Entovis Triple Chamber Pacemaker
Lead sponsor
Biotronik SE & Co. KG
Phase
Observational
Overall status
Completed
Start date
June 30, 2013
Completion date
September 30, 2015
Enrollment
174 (actual)
Sites
23

Conditions

As the registry lists them; a condition with its own page is linked.

safety of mr (magnetic resonance) conditional crt-pacemakers and icds