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Buflomedil in Arterial Occlusive Disease: Results of a Controlled Multicenter StudyMedizinische Universitäts-Poliklinik, Bonn, Federal Republic of Germany
Evangelisches Krankenhaus Mülheim, Rühr, Federal Republic of Germany
Knappschaftskrankenhaus Bottrop, Bottrop, Federal Republic of Germany
Abteilung fur Dermatologie und Angiologie der Universitäts-Kliniken Essen, Essen, Federal Republic of Germany
Johannes-Hospital Duisburg, Duisburg, Federal Republic of Germany
Marienhospital y Gelsenkirchen, Gelsenkirchen, Federal Republic of Germany
Marienhospital y Gelsenkirchen, Gelsenkirchen, Federal Republic of Germany
Institut für Forschungsplanung - CH Bettingen-Basel, Switzerland In a double-blind, randomised multicentre study buflomedil, a vasoactive substance, was compared with placebo in the treatment of 93 patients with chronic arterial occlusive disease. After a run-in period of four weeks the patients received either buflomedil (600 mg daily) or placebo over 12 weeks. The pain-free and the total walking distances improved significantly in both groups. However, the differences in the improvement between the two groups were highly signifi cant and in favour of buflomedil: for the pain-free walking distance p<0.001 and for the total walking distance p<0.01. The results indicate that buflomedil has a beneficial effect on the symptoms and lengthens the walking distance in patients with arterial occlusive disease.
Angiology, Vol. 35, No. 8,
500-505 (1984) |
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