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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)