A Safety and Efficacy Study of Blood Pressure Control in Acute Aortic Emergencies - A Pilot Study (PROMPT)

PHASE4TerminatedINTERVENTIONAL
Enrollment

5

Participants

Timeline

Start Date

November 30, 2009

Primary Completion Date

August 31, 2012

Study Completion Date

August 31, 2012

Conditions
Aortic AneurysmAortic Disease
Interventions
DRUG

clevidipine.

Clevidipine administered per IV infusion, starting dose of 2 mg/h (4 mL/hr) for 3 minutes \& titrated to the desired BP lowering effect to SBP goal of \< 120 mmHg, max infusion rate may not exceed 32 mg/h (64 mL/hr).

Trial Locations (1)

77030

The Methodist Hospital, Houston

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

The Medicines Company

INDUSTRY

collaborator

The Methodist Hospital Research Institute

OTHER

lead

Asma Zainab, M.D.

OTHER