Clinical trial

Magnevist® Injection Enhanced MRA at Two Dose Levels Compared to Non Contrast…

NCT00185276 · Bayer, Industry · Completed

Key facts

NCT number NCT00185276
Title Magnevist® Injection Enhanced MRA at Two Dose Levels Compared to Non Contrast MRA for the Detection of Structural Abnormalities of the Infrarenal Aorta and Peripheral Arteries
Official title Randomized, Multi-center Open Label Study of the Safety (Open-label) and Efficacy (Open-label & Blinded Reader) of Magnevist® Injection-enhanced Magnetic Resonance Arteriography (MRA) at Two Dose Levels and 2-dimensional-time-of-flight (2D-TOF) MRA in Patients Undergoing MRA of the Infrarenal Aorta…
Lead sponsor Bayer, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Peripheral Vascular Disease
Intervention type Drug
Interventions Gadopentetate dimeglumine (Magnevist, BAY86-4882)
Enrollment 365
Start date Mar 1, 2003
Completion Aug 1, 2004
First posted Sep 16, 2005
Last update posted Dec 30, 2014

At a glance

  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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