Non-interventional Comparison of Sedatives on Weaning From Mechanical Ventilation in Intensive Care Patients — NICEWEAN  

Critical Illness Clinical Trial

Official title: Non-interventional Comparison of Sedatives on Weaning From Mechanical Ventilation in Intensive Care Patients

Status Terminated

Clinical Trial Summary

The purpose of this study is to determine whether the use of different sedatives affect the weaning process from mechanical ventilation in intensive care patients.

Clinical Trial Description

Traditionally patients with ongoing mechanical ventilation have been sedated to assure absence of pain, anxiety and to provide comfort. Unfortunately this approach might have negative consequences such as prolonged time for mechanical ventilation, length of stay in the ICU and hospital.

In this study, the investigators would like to investigate (in an exploratory way due to the non-interventional setup) whether weaning from mechanical ventilation will be affected by the choice of sedatives - including dexmedetomidine, midazolam and propofol. This study also aims at investigating how the choice of primary sedative will affect delirium/anxiety, need of other medications (sedatives, analgesics, anti-psychotics), quality of life after ICU and the presence of Post-Traumatic Stress Disorder. In addition, the investigators aim at receiving information from the caregivers on their ICU experience, as recent data imply that not only the ICU patient but also the caregiver suffer from PTSD after the ICU stay. ;

Related Conditions & MeSH terms

• Critical Illness

• NCT number: NCT01707680
• Study type: Observational
• Source: Orion Corporation, Orion Pharma
• Status: Terminated
• Start date: June 1, 2012
• Completion date: November 1, 2015