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
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.
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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