Clevidipine in the Treatment of Patients With Severe Hypertension (VELOCITY)

PHASE3CompletedINTERVENTIONAL
Enrollment

131

Participants

Timeline

Start Date

September 30, 2006

Primary Completion Date

January 31, 2007

Study Completion Date

February 28, 2007

Conditions
Hypertension
Interventions
DRUG

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..

Trial Locations (14)

16550

Hamot Shock Trauma, Erie

19107

Pennsylvania Hospital, Philadelphia

20037

The George Washington University Medical Center, Washington D.C.

21239

Good Samaritan Hospital, Baltimore

27710

Duke University Medical Center, Durham

36106

Jackson Hospital, Montgomery

43606

The Toledo Hospital, Toledo

44109

Metrohealth Medical Center, Cleveland

44195

The Cleveland Clinic, Cleveland

70118

Louisiana State University Medical Center/Charity Hospital, New Orleans

71103

Critical Care Research Center at Louisiana State University Health Sciences Center, Shreveport

77030

The University of Texas Health Science Center, Houston

90073

VA Medical Center W. LA, Los Angeles

97225

Providence Heart & Vascular Institute, d/b/a Providence St. Vincent Medical Center, Portland

Sponsors
All Listed Sponsors
lead

The Medicines Company

INDUSTRY