Delirium Clinical Trial
Official title:
Comparison of Sedative Effects of Sevoflurane, Propofol and Dexmedetomidine on the Clinical Course of Delirium and Neuroinflammation in Mechanically Ventilated Patients
Assessment of sedative effects of sevoflurane, dexmedetomidine and propofol on the clinical course of delirium, SIRS and neuroinflammation in mechanically ventilated patients using CAM-ICU scale, GSK-3beta and protein S100b in serum.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | August 2018 |
Est. primary completion date | May 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility |
Inclusion Criteria: - presence of delirium Exclusion Criteria: - presence of Alzheimer's disease - any mental disorder - presence of cancer |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Moscow Regional Research and Clinical Institute Moniki n.a. M.F. Vladimirskiy |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Duration of Delirium | Delirium assessment by CAM-ICU scale | up to 5 days | |
Secondary | Change of protein S100b in serum | from delirium onset up to 5 days | ||
Secondary | Change of GSK-3beta in serum | from delirium onset up to 5 days |
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