drugset / Trial / NCT00652418
Magnevist (SH L 451A) Intra-individual Dose Comparison Study in Magnetic Resonance Angiography
RandomizedCrossoverOpen-labelDiagnostic
Summary
The objective of the study was to compare the efficacy of Magnevist (SH L 451 A) at doses of 0.1 mmol/kg and 0.2 mmol/kg in contrast-enhanced 3D-Magnetic Resonance Angiography in three regions (abdominal, femoral, and leg regions) for visualization of arteries, evaluating 179 not assessable: caused by contrast media in the evaluation of structural abnormalities. Magnevist (SH L 451 A) was administered intravenously in a crossover design in patients with arterial disease in the abdominal to leg regions. The safety of the 0.2 mmol/kg dose was also assessed.
Timeline
- Start
- 2004-07
- Primary completion
- 2004-10
- Completion
- 2004-10
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Gadopentetate dimeglumine | Diagnostic / imaging agent | 0.1 unknown | Intravenous |
| Subject | Gadopentetate dimeglumine | Diagnostic / imaging agent | 0.2 unknown | Intravenous |