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GARDIAN, Gadovist in Routine Diagnostic Magnetic Resonance Imaging Administration in Non-selected Patients — GARDIAN  

Magnetic Resonance Imaging Clinical Trial

Official title:
GARDIAN, Gadovist in Routine Diagnostic Magnetic Resonance Imaging Administration in Non-selected Patients

Clinical Trial Summary

Prospective, non-interventional, multi-center study. The observation period for each subject covers the treatment period with Gadovist®. For each patient, the treating physician or nurse documents demographics, medical data, safety parameters and treatment signs and symptoms at the visit. Patients with severe renal impairment will be followed-up after 3 month by phone call from the investigator if in line with routine practice. Data audit/monitoring by source data verification will be done in a subset of sites and patients

Clinical Trial Description

Evaluate the safety and tolerability of Gadovist in patients requiring contrast-enhanced MRI. ;

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01095081
Study type Observational
Source Bayer
Contact
Status Completed
Phase N/A
Start date July 2010
Completion date April 2013
View Details
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