Bien S, Schumacher M, Berger W, Wenzel-Hora B I
Fortschr Geb Rontgenstrahlen Nuklearmed Erganzungsbd. 1989;128:158-60.
As part of a clinical Phase III study of the nonionic, dimeric contrast medium iotrolan, differences in opacification, tolerance, and effects on the electroencephalogram after myelography were examined in a double-blind comparison with iohexol. Two groups of 25 patients each received either 10 ml iotrolan 240 mg I/ml or 10 ml iohexol 240 mg I/ml for lumbar myelography, and two groups of 50 patients each received either 10 ml iotrolan 300 mg I/ml or 10 ml iohexol 300 mg I/ml for lumbar, thoracic or cervical myelography. The overall assessment of the opacification in the subarachnoid space, which was moderate in only one case of each group and otherwise good, showed no differences between the preparations. The tolerance of both concentrations of iotrolan proved to be significantly better than those of iohexol: at a significance level in the chi-square test of p less than 0.001 in a simple size of 25 patients per preparation with 240 mg I/ml and at a significance level of p +/- 0.05 in a sample size of 50 patients per preparation with 300 mg I/ml.
作为非离子二聚体造影剂碘曲仑的一项临床III期研究的一部分,在与碘海醇的双盲对比中,对脊髓造影后的造影清晰度、耐受性及对脑电图的影响差异进行了检查。两组各25例患者分别接受10 ml 240 mg I/ml的碘曲仑或10 ml 240 mg I/ml的碘海醇进行腰椎脊髓造影,两组各50例患者分别接受10 ml 300 mg I/ml的碘曲仑或10 ml 300 mg I/ml的碘海醇进行腰段、胸段或颈段脊髓造影。蛛网膜下腔造影清晰度的总体评估显示,每组仅1例为中等,其余均良好,两种制剂之间无差异。两种浓度碘曲仑的耐受性均明显优于碘海醇:在每种制剂25例患者的样本量下,碘曲仑2 ml 240 mg I/ml时卡方检验的显著性水平p小于0.001;在每种制剂50例患者的样本量下,碘曲仑300 mg I/ml时显著性水平为p±0.05。