Drug Use Investigation of Gadovist.

Status Completed

Clinical Trial Summary

The objectives of this study are to investigate the safety and effectiveness of Gadovist.

Clinical Trial Description

This is a prospective, non-interventional, continuous submission safety study that includes patients who planned Gadolinium (Gd) contrast enhanced Magnetic Resonance Imaging (MRI) in accordance with approved label. The investigator will have made the choice of Gd enhanced MRI (the decision to use Gadovist according the Japanese Package Insert prior to enrolling the patient in this study). The study period is 3 years. Data analysis period is 1 year. In total, 3300 patients will be recruited. For each patient, data are collected as defined in the case report form (CRF) at the visit for MRI examination (as per investigators routine practice). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02540967
Study type	Observational
Source	Bayer
Contact
Status	Completed
Phase
Start date	October 27, 2015
Completion date	November 2, 2017

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