Testing the Feasibility of Patient Controlled Sedation for Ventilated ICU Patients

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

15

Participants

Timeline

Start Date

March 31, 2013

Primary Completion Date

July 31, 2014

Study Completion Date

July 31, 2015

Conditions
Acute Respiratory FailureAnxiety
Interventions
DRUG

Dexmedetomidine

loading dose (0.5 mcg/kg i.v.), followed by a continuous basal infusion (0.2-0.7 mcg/kg/hr) with 3 allowable patient-controlled self-boluses per hour (0.25 mcg/kg) each with a 20-minute lock-out. Study infusion up to 5 days.

Trial Locations (1)

55455

University of Minnesota Medical Center, Minneapolis

All Listed Sponsors
collaborator

National Institute of Nursing Research (NINR)

NIH

collaborator

Hospira, now a wholly owned subsidiary of Pfizer

INDUSTRY

lead

University of Minnesota

OTHER

NCT01606852 - Testing the Feasibility of Patient Controlled Sedation for Ventilated ICU Patients | Biotech Hunter | Biotech Hunter