Clinical and biological activity of the antiplatelet agent suloctidil in treatment of idiopathic recurrent vein thrombosis (I.R.V.T.)

Thromb Haemost. 1982 Feb 26;47(1):27-31.

Abstract

A double blind cross over study with suloctidil (Sulocton, Continental Pharma) and placebo was carried out for 6 months in 31 patients with idiopathic recurrent vein thrombosis. They were previously unsuccessfully treated with vitamin K antagonists (VKA) (18 patients) or acetylsalicylic acid (ASA) (13 patients) combined or not the a fibrinolysis activator (theophylline nicotinate). Clinical features, ultrasonic venous flow and biological parameters were controlled monthly during the 6 month treatment. Relevant improvement of clinical, ultrasonic and biological parameters was only observed under suloctidil therapy: during placebo administration 12 patients developed new thrombotic events complicated in 2 by pulmonary embolism while none occurred under suloctidil therapy.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Antigens
  • Blood Platelets / drug effects*
  • Cell Survival
  • Factor VIII / immunology
  • Female
  • Humans
  • Male
  • Middle Aged
  • Platelet Factor 4
  • Platelet Function Tests
  • Propanolamines / therapeutic use*
  • Pulmonary Embolism / complications
  • Recurrence
  • Suloctidil / therapeutic use*
  • Thrombophlebitis / complications
  • Thrombophlebitis / diagnosis
  • Thrombophlebitis / drug therapy*
  • Ultrasonography
  • Vitamin K / antagonists & inhibitors
  • beta-Thromboglobulin

Substances

  • Antigens
  • Propanolamines
  • beta-Thromboglobulin
  • Vitamin K
  • Platelet Factor 4
  • Factor VIII
  • Suloctidil