Phase
Condition
N/ATreatment
Propofol-remifentanil
Routine sedation and analgesia
Dexmedetomidine-esketamine
Clinical Study ID
Ages > 50 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Aged 50 years or older;
Admitted to the intensive care unit (ICU) after surgery;
Receiving mechanical ventilation or high-flow nasal cannula oxygen therapy duringnight-time (after 6 pm), with an expected duration of ≥12 hours.
Exclusion
Exclusion Criteria:
Duration of invasive/non-invasive ventilation ≥12 hours before enrollment;
Planning to receive muscle relaxant treatment;
History of schizophrenia, epilepsy, Parkinson's disease, or myasthenia gravis;
Unable to communicate due to coma, delirium, severe dementia, or language barrierbefore receiving mechanical ventilation or high-flow nasal cannula oxygen therapy;
Acute stroke or hypoxic encephalopathy, or after craniocerebral injury orneurosurgery;
Comorbid with hyperthyroidism or pheochromocytoma;
Taking sedative/hypnotic drugs or analgesics regularly (for more than 1 week) in thelast month;
LVEF<30%; sick sinus syndrome, severe sinus bradycardia (heart rate<50 beats/min),atrioventricular block of more than II degree and without pacemaker; or systolicblood pressure <90 mmHg despite vasopressor infusion;
Severe liver dysfunction (Child-Pugh C grade), severe renal dysfunction (dialysis),or estimated survival ≤24 hours;
Diagnosed obstructive sleep apnea, or body mass index >30 kg/m2;
Allergies to dexmedetomidine and/or esketamine, or other conditions that areconsidered unsuitable for study participation;
Enrolled in other clinical studies.
Study Design
Study Description
Connect with a study center
Peking University First Hospital
Beijing, Beijing 100034
ChinaSite Not Available
Peking University First Hospital
Beijing 1816670, Beijing Municipality 2038349 100034
ChinaSite Not Available

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