213
Participants
Start Date
January 31, 2008
Primary Completion Date
November 30, 2008
Study Completion Date
November 30, 2008
IV Acetaminophen
Arm 1: 1 g IV Acetaminophen every 6 hours administered for five days. Arm 2: 650 mg IV Acetaminophen every 4 hours administered for five days. Arm 3: The standard of care treatments were defined as any medication the investigator deemed appropriate to treat the subject, including products containing acetaminophen but excluding IV acetaminophen.
Weill Medical College of Cornell University, New York
Thomas Jefferson University, Philadelphia
University of Miami School of Medicine, Miami
Nature Coast Clinical Research, Crystal River
G&G Research, Ft. Pierce
The Ohio State University Medical Center, Columbus
Memorial Herman/Memorial City Hospital, Houston
Arcadia Methodist Hospital, Arcadia
Huntington Memorial Hospital, Pasadena
Lotus Clinical Research, Inc., Pasadena
Glendale Adventist Medical Center, Glendale
Accurate Clinical Trials, Inc., Laguna Hills
Santa Barbara Cottage Hospital, Santa Barbara
Oregon Health Science University, Portland
Lead Sponsor
Mallinckrodt
INDUSTRY