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Clinical Trials/ACTRN12620001088932
ACTRN12620001088932
Recruiting
Phase 4

The effect of Early Sedation with Dexmedetomidine vs. Placebo on 90-day mortality in Older Ventilated Critically Ill Patients. A Prospective, Multi-Centre, Double-Blind, Randomized, Controlled Trial

Monash University0 sites3,500 target enrollmentOctober 20, 2020

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Critically ill patients
Sponsor
Monash University
Enrollment
3500
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 20, 2020
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\.Age is equal to or older than 65 years
  • 2\.Intubated and receiving invasive mechanical ventilation in an intensive care unit
  • 3\.The treating clinicians believe that the patient will remain intubated and ventilated until the day after tomorrow (unlikely to be extubated next day)
  • 4\.The patient requires immediate ongoing sedative medication for comfort, safety and to facilitate the delivery of life support measures.

Exclusion Criteria

  • 1\.Has been intubated (excluding time spent intubated within an operating theatre or transport) for greater than 12 hours in an intensive care unit
  • 2\.Proven or suspected acute primary brain lesion such as traumatic brain injury, intracranial haemorrhage, stroke, or hypoxic brain injury
  • 3\.Proven or suspected spinal cord injury or other pathology that may result in permanent or prolonged weakness
  • 4\.Admission with a suspected or proven drug overdose or burns.
  • 5\.Administration of ongoing neuromuscular blockade
  • 6\.Mean arterial blood (MAP) pressure that is less than 50 mmHg despite adequate resuscitation and vasopressor therapy at time of randomization
  • 7\.Heart rate less than 55 beats per minute unless the patient is being treated with a betablocker or a high grade atrio\-ventricular block in the absence of a functioning pacemaker
  • 8\.Known sensitivity to dexmedetomidine
  • 9\.Acute fulminant hepatic failure
  • 10\.Receiving full time residential nursing care

Outcomes

Primary Outcomes

Not specified

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