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Naftidrofuryl in chronic arterial disease. Results of a controlled multicenter study.

Abstract
In a double blind, randomized multicenter study naftidrofuryl, a vasoactive substance, was compared with placebo in the treatment of 104 patients with chronic arterial occlusive disease. After a run-in period of four weeks the patients received either naftidrofuryl (600 mg daily) or placebo over 12 weeks. The pain-free and the total walking distances improved significantly in both groups. However, the difference in the improvement of the pain-free walking distance was significant (p less than 0.02) in favour of naftidrofuryl. There also was a difference in the improvement of the total walking distance in favour of naftidrofuryl which was not significant. The results indicate that naftidrofuryl has a beneficial effect on the symptoms and lengthens the painfree walking distance in patients with arterial occlusive disease.
AuthorsG Trübestein, H Böhme, H Heidrich, F Heinrich, H Hirche, U Maass, H Mörl, G Rudofsky
JournalAngiology (Angiology) Vol. 35 Issue 11 Pg. 701-8 (Nov 1984) ISSN: 0003-3197 [Print] United States
PMID6388425 (Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial)
Chemical References
  • Furans
  • Placebos
  • Nafronyl
Topics
  • Adult
  • Arterial Occlusive Diseases (drug therapy)
  • Blood Flow Velocity
  • Blood Pressure
  • Chronic Disease
  • Clinical Trials as Topic
  • Double-Blind Method
  • Female
  • Furans (therapeutic use)
  • Humans
  • Male
  • Middle Aged
  • Nafronyl (therapeutic use)
  • Placebos
  • Statistics as Topic

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