Status:
COMPLETED
Responsiveness Index Versus the RASS Based Method for Adjusting Sedation in Critically Ill Patients
Lead Sponsor:
Helsinki University Central Hospital
Conditions:
Critical Illness
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
Systematic evaluation of pain, agitation and delirium in ICU-patients is recommended and deep sedation should be avoided. Sedation is still monitored with clinical assessments, like RASS. The Responsi...
Detailed Description
Sedation of intensive care patients is needed for patient's safety but deep sedation is associated with adverse outcomes. Frontal electromyogram based Responsiveness Index (RI) aims to quantify patien...
Eligibility Criteria
Inclusion
- Intensive care patients
- Need of mechanical ventilation and sedation
Exclusion
- contraindication to propofol or oxycodone
- hypoxic or traumatic brain injury
- intracranial hemorrhage
- status epilepticus
- drug overdose as admission diagnosis
Key Trial Info
Start Date :
March 1 2013
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 28 2017
Estimated Enrollment :
32 Patients enrolled
Trial Details
Trial ID
NCT03250481
Start Date
March 1 2013
End Date
August 28 2017
Last Update
August 15 2019
Active Locations (1)
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1
HelsinkiUCH
Helsinki, Finland