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DOI: 10.1055/s-2008-1065351
© Georg Thieme Verlag KG Stuttgart · New York
Benfotiamine in Diabetic Polyneuropathy (BENDIP): Results of a Randomised, Double Blind, Placebo-controlled Clinical Study
Publication History
received 28.11.2007
first decision 08.01.2008
accepted 11.03.2008
Publication Date:
13 May 2008 (online)
Abstract
Aim: Efficacy and safety of benfotiamine in treatment of diabetic polyneuropathy.
Methods: Double blind, placebo-controlled, phase-III-study. 181 patients were screened. 165 patients with symmetrical, distal diabetic polyneuropathy were randomised to one of three treatment groups entering the wash-out phase and 133/124 patients were analysed in the ITT/PP analysis: Benfotiamine 600 mg per day (n=47/43), benfotiamine 300 mg per day (n=45/42) or placebo (n=41/39).
Results: After 6 weeks of treatment, the primary outcome parameter NSS (Neuropathy Symptom Score) differed significantly between the treatment groups (p=0.033) in the PP (per protocol) population. In the ITT (intention to treat) population, the improvement of NSS was slightly above significance (p=0.055). The TSS (Total Symptom Score) showed no significant differences after 6 weeks of treatment. The improvement was more pronounced at the higher benfotiamine dose and increased with treatment duration. In the TSS, best results were obtained for the symptom “pain”. Treatment was well tolerated in all groups.
Conclusion: Benfotiamine may extend the treatment option for patients with diabetic polyneuropathy based on causal influence on impaired glucose metabolism. Further studies should confirm the positive experiences.
Key words
diabetic polyneuropathy - benfotiamine - advanced glycation end products - glucose metabolism
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Correspondence
Prof. Dr. H. Stracke
University Hospital Giessen and Marburg GmbH
Medical Clinic and Policlinic III
Rodthohl 6
35392 Giessen
Germany
Phone: +49/641/994 27 54
Fax: +49/641/994 27 69
Email: Hilmar.Stracke@innere.med.uni-giessen.de