80
Participants
Start Date
July 31, 2011
Primary Completion Date
January 31, 2012
Study Completion Date
January 31, 2012
Nefopam
The nefopam group received 120 mg nefopam (Acupan, Pharmbio, France) by continuous iv infusion over the study period (48h)
saline solution
The Control group received 120 mg placebo infusion (saline solution) by continuous iv infusion over the study period (48h).
Centre Hospitalier Universitaire de Nīmes
OTHER