19
Participants
Start Date
January 31, 2003
Primary Completion Date
April 30, 2004
Study Completion Date
April 30, 2004
Enoxaparine
al patients received additional low molecular heparin, if the safety cohort of three patients received at least 4 weeks of combined treatment without severe side effects, recruitment were continued until a minimum of 15 patients completed at least 3 months of treatment.
Charité - Universitätsmedizin Berlin, Berlin
CONKO-Studiengruppe
OTHER