Effects of defibrotide in patients with chronic deep insufficiency. The PROVEDIS study

S. Coccheri, G. M. Andreozzi, M. D'addato, G. F. Gensini

Research output: Contribution to journalArticlepeer-review


Aim. In the present study the effect of defibrotide, an anti-thrombotic and profibrinolytic agent, was investigated in patients with chronic venous insufficiency (CVI) due to deep vein obstruction and/or reflux (chronic deep vein insufficiency, CDVI). Methods. The study was a multicenter, randomized, double blind placebo controlled trial in which only patients with CDVI confirmed by ultrasound were enrolled. All patients were treated with adequate elastic compression and randomized to receive either oral defibrotide (800 mg/die) or matching placebo for 1 year. Patients with active or previous leg ulcer were excluded. Results. A total of 288 patients were randomized and 159 completed the study. At baseline ultrasound investigation, obstructive changes were found in 2/3 of all patients thus ascertaining a post-thrombotic syndrome (PTS). The primary endpoint, ankle circumpherence, was significantly reduced under defibrotide from day 120 throughout 360. Scores for pain and edema were improved. The number of episodes of superficial thrombophlebitis and deep vein thrombosis was significantly lower under defibrotide (n=2) than under placebo (n=10). The majority of these events occurred in the subset of patients with documented PTS. Conclusion. Treatment with defibrotide in addition to elastic compression in patients with objectively assessed CDVI, mostly due to PTS, resulted in clinical benefits and prevented thrombotic complications harmful to the limb conditions.

Original languageEnglish
Pages (from-to)100-107
Number of pages8
JournalInternational Angiology
Issue number2
Publication statusPublished - Jun 2004


  • Fibrinolytic agents
  • Venous insufficiency, therapy
  • Venous thrombosis

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine


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