131
Participants
Start Date
September 30, 2006
Primary Completion Date
January 31, 2007
Study Completion Date
February 28, 2007
clevidipine
Clevidipine was required to be administered continuously for a minimum of 18 hours and a maximum of 96 hours and was not to exceed a rate of 32.0 mg/h at any time. Use of an additional or alternative intravenous antihypertensive agent was allowed if the blood pressure target range was not achieved or maintained. If transition to an oral antihypertensive agent is required, then approximately 1 hour prior to the anticipated cessation of clevidipine infusion, but no less than at the 18-hour time point, an oral antihypertensive agent was allowed to be administered as clevidipine was down-titrated or terminated as needed in order to achieve the desired blood pressure level..
Hamot Shock Trauma, Erie
Pennsylvania Hospital, Philadelphia
The George Washington University Medical Center, Washington D.C.
Good Samaritan Hospital, Baltimore
Duke University Medical Center, Durham
Jackson Hospital, Montgomery
The Toledo Hospital, Toledo
Metrohealth Medical Center, Cleveland
The Cleveland Clinic, Cleveland
Louisiana State University Medical Center/Charity Hospital, New Orleans
Critical Care Research Center at Louisiana State University Health Sciences Center, Shreveport
The University of Texas Health Science Center, Houston
VA Medical Center W. LA, Los Angeles
Providence Heart & Vascular Institute, d/b/a Providence St. Vincent Medical Center, Portland
Lead Sponsor
The Medicines Company
INDUSTRY