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マグネビスト(SH L 451A)の磁気共鳴血管造影における個体内用量比較試験
基本情報
- NCT ID
- NCT00652418
- ステータス
- 完了
- 試験のフェーズ
- 第2相
- 試験タイプ
- 介入
- 目標被験者数
- 12
- 治験依頼者名
- Bayer
概要
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.
対象疾患
Magnetic Resonance AngiographyPeripheral Vascular DiseasesPeripheral Arterial Diseases
介入
Gadopentetate dimeglumine (Magnevist, BAY86-4882, SH L 451A)(DRUG)
Gadopentetate dimeglumine (Magnevist, BAY86-4882, SH L 451A)(DRUG)
依頼者(Sponsor)
バイエル薬品株式会社(INDUSTRY)