Study to Evaluate The Analgesic Efficacy and Safety of Intravenous Paracetamol in Subjects With Postoperative Pain After Total Hip Arthroplasty

PHASE4CompletedINTERVENTIONAL
Enrollment

86

Participants

Timeline

Start Date

April 30, 2006

Primary Completion Date

February 29, 2008

Study Completion Date

February 29, 2008

Conditions
Pain
Interventions
DRUG

Paracetamol

IV Solution, Intravenous, 100 mL (10 mg/mL), 4 times at 6-hour intervals, 24 hours

DRUG

Placebo

IV Solution, Intravenous, 100 mL (0 mg/mL), 4 times at 6-hour intervals, 24 hours

Trial Locations (5)

28007

Local Institution, Madrid

28041

Local Institution, Madrid

28922

Local Institution, Alcorcón

48903

Local Institution, Vizcaya

08024

Local Institution, Barcelona

Sponsors
All Listed Sponsors
lead

Bristol-Myers Squibb

INDUSTRY