Dexmedetomidine-Esketamine Combination for Sedation and Analgesia in ICU Patients
Effect of Dexmedetomidine-Esketamine Combination for Sedation and Analgesia on Delirium in ICU Patients With Mechanical Ventilation: A Multicenter Randomized Trial
1 other identifier
interventional
1,508
1 country
3
Brief Summary
Patients with mechanical ventilation in the intensive care unit (ICU) often develop anxiety and agitation, sleep distuebances, and delirium. Delirium occurrence is associated with worse early and long-term outcomes. Dexmedetomidine and ketamine are recommended for sedation and analgesia in ICU patients, but each may induce side effects. The sedative effects of dexmedetomidine can help mitigate the psychiatric side effects of esketamine. Recent studies showed that dexmedetomidine-esketamine combination improved analgesia and sleep quality without increasing psychiatric side effects. This trial is designed to test the hypothesis that dexmedetomidine-esketamine combination for sedation and analgesia in ICU patients with mechanical ventilation may reduce delirium and improve respiratory recovery.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Nov 2025
Longer than P75 for not_applicable
3 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 15, 2024
CompletedFirst Posted
Study publicly available on registry
June 21, 2024
CompletedStudy Start
First participant enrolled
November 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2029
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2030
July 31, 2025
July 1, 2025
4.1 years
June 15, 2024
July 28, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Incidence of delirium within 7 days
Delirium is assessed twice daily with the Confusion Assessment Method for the Intensive Care Unit (CAM-ICU) or the 3-Minute Diagnostic Assessment for Delirium using the Confusion Assessment Method (3D-CAM) during the 7-day period after enrollment or until hospital discharge. Positive result of delirium assessments at any timepoint is defined as occurrence of delirium.
Up to 7 days after enrollment
Secondary Outcomes (4)
Days alive without delirium or come during the 7-day period
Up to 7 days after enrollment
Ventilator-free days within 30 days
Up to 30 days after enrollment
Length of stay in the ICU
Up to 30 days after enrollment
30-day all-cause mortality
Up to 30 days after enrollment
Other Outcomes (6)
Proportion of patients without delirium
Up to 7 days after enrollment
Proportion of patients without delirium or coma
Up to 7 days after enrollment
Length of stay in hospital after enrollment
Up to 30 days after enrollment
- +3 more other outcomes
Study Arms (2)
Dexmedetomidine-Esketamine Combination
EXPERIMENTALSedation-analgesia is provided with dexmedetomidine-esketamine combination for up to 14 days or until discharge from the ICU. The formulation consists of dexmedetomidine 200 μg/2 ml and esketamine 100 mg/4 ml, diluted with normal saline to a total volume of 50 ml, resulting in a dexmedetomidine concentration of 4 μg/ml and an esketamine concentration of 2 mg/ml.
Dexmedetomidine
ACTIVE COMPARATORSedation-analgesia is provided with dexmedetomidine for up to 14 days or until discharge from the ICU. The formulation consists of dexmedetomidine 200 μg/2 ml, diluted with normal saline to a total volume of 50 ml, resulting in a dexmedetomidine concentration of 4 μg/ml.
Interventions
For patients with invasive ventilation, nighttime sedation (20:00-06:00) is provided with an initial infusion rate of \[0.05Ă—kg\] ml/h which is increased by \[0.025Ă—kg\] ml/h every 10 min, until the Richmond Agitation-Sedation Scale (RASS) reaches -2 to -1, maximal infusion rate reaches \[0.175Ă—kg\] ml/h, or adverse reactions occur. Daytime sedation (06:00-20:00) is provided as above when considered necessary by the ICU physicians, with a target RASS score of -2 to +1. For patients with non-invasive ventilation (including high-flow nasal oxygenation) or without assisted ventilation, nighttime sedation (20:00-06:00) is provided with an initial infusion rate of \[0.0125Ă—kg\] ml/h which is increased by \[0.0125Ă—kg\] ml/h every 10 min, until the RASS reaches -1, maximal infusion rate reaches \[0.05Ă—kg\] ml/h, or adverse reactions occur. Daytime sedation (06:00-20:00) is typically not required but is provided when considered necessary by the ICU physicians, with a target RASS score of -1 to +1.
For patients with invasive ventilation, nighttime sedation (20:00-06:00) is provided with an initial infusion rate of \[0.05Ă—kg\] ml/h which is increased by \[0.025Ă—kg\] ml/h every 10 min, until the Richmond Agitation-Sedation Scale (RASS) reaches -2 to -1, maximal infusion rate reaches \[0.175Ă—kg\] ml/h, or adverse reactions occur. Daytime sedation (06:00-20:00) is provided as above when considered necessary by the ICU physicians, with a target RASS score of -2 to +1. For patients with non-invasive ventilation (including high-flow nasal oxygenation) or without assisted ventilation, nighttime sedation (20:00-06:00) is provided with an initial infusion rate of \[0.0125Ă—kg\] ml/h which is increased by \[0.0125Ă—kg\] ml/h every 10 min, until the RASS reaches -1, maximal infusion rate reaches \[0.05Ă—kg\] ml/h, or adverse reactions occur. Daytime sedation (06:00-20:00) is typically not required but is provided when considered necessary by the ICU physicians, with a target RASS score of -1 to +1.
Eligibility Criteria
You may qualify if:
- Aged ≥18 years;
- Receiving invasive or non-invasive mechanical ventilation in the ICU, with an expected duration ≥24 hours;
- Require sedation as judged by ICU physicians.
You may not qualify if:
- Pregnant or lactating women;
- History of schizophrenia, epilepsy, Parkinson's disease, or myasthenia gravis;
- Unable to communicate due to coma, severe dementia, or language barrier prior to invasive/non-invasive mechanical ventilation;
- After stroke, hypoxic encephalopathy, traumatic brain injury, or neurosurgery;
- Comorbid with hyperthyroidism or pheochromocytoma;
- Left ventricular ejection fraction \<30%, sick sinus syndrome, severe sinus bradycardia (heart rate \<50 bpm), second-degree or higher atrioventricular block without a pacemaker, or systolic blood pressure \<90 mmHg despite use of vasopressors;
- Severe liver dysfunction (Child-Pugh Class C), severe renal dysfunction (requiring dialysis), or expected survival ≤24 hours;
- Allergy to dexmedetomidine and/or esketamine, or any other conditions that are considered unsuitable for study participation.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (3)
Peking University First Hospital
Beijing, Beijing Municipality, 100034, China
Peking University International Hospital
Beijing, Beijing Municipality, 102206, China
Tianjin Medical University General Hospital
Tianjin, Tianjin Municipality, 300052, China
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PMID: 21818162BACKGROUND
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Dong-Xin Wang, MD, PhD
Peking University First Hospital
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- QUADRUPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor and Chairman, Department of Anesthesiology
Study Record Dates
First Submitted
June 15, 2024
First Posted
June 21, 2024
Study Start
November 1, 2025
Primary Completion (Estimated)
December 1, 2029
Study Completion (Estimated)
December 1, 2030
Last Updated
July 31, 2025
Record last verified: 2025-07
Data Sharing
- IPD Sharing
- Will not share