Overview

Reducing Delirium After Cardiac Surgery: A Multifaceted Approach Of Perioperative Care

Status:
Completed
Trial end date:
2015-04-01
Target enrollment:
0
Participant gender:
All
Summary
The objective of this study is to reduce the incidence of postoperative delirium after cardiac surgery in the elderly patient. This proposal is a clinical trial designed to reduce delirium in patients undergoing cardiac surgery by replacing standard postoperative sedation protocols (propofol, midazolam, opioids) with a new alpha2-adrenergic receptor agonist (dexmedetomidine) possessing sedative, analgesic, and antinociceptive properties. Resource utilization analysis will be performed to determine cost effectiveness of the new treatment modality.
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University Health Network, Toronto
Collaborators:
Hospira, Inc.
Hospira, now a wholly owned subsidiary of Pfizer
Treatments:
Dexmedetomidine
Propofol
Criteria
Inclusion Criteria:

- Age ≥60 years, undergoing high risk cardiac surgery, signed informed consent.

Exclusion Criteria:

- Patients with symptomatic cerebrovascular disease, history of delirium, schizophrenia
or preoperative use of psychotropic medications.