NCT03250481View on ClinicalTrials.gov

Responsiveness Index Versus the RASS Based Method for Adjusting Sedation in Critically Ill Patients

NACompletedINTERVENTIONAL
Enrollment

32

Participants

Timeline

Start Date

March 31, 2013

Primary Completion Date

August 28, 2017

Study Completion Date

August 28, 2017

Conditions
Critical Illness
Interventions
DRUG

Propofol

Sedation targeted to RASS -3-0 or RI 20-40

Trial Locations (1)

Unknown

HelsinkiUCH, Helsinki

All Listed Sponsors
lead

Helsinki University Central Hospital

OTHER

NCT03250481 - Responsiveness Index Versus the RASS Based Method for Adjusting Sedation in Critically Ill Patients | Biotech Hunter | Biotech Hunter