Mini-dose Dexmedetomidine-Esketamine Infusion and Perioperative Sleep Quality
Effect of Mini-dose Dexmedetomidine-Esketamine Infusion on Sleep Quality in Older Patients Undergoing Knee or Hip Replacement Surgery: A Multicenter Randomized Controlled Trial
1 other identifier
interventional
154
1 country
2
Brief Summary
Sleep disturbances are prevalent in older patients with osteoarthrosis or fracture who are scheduled for knee or hip replacement surgery. The occurrence of sleep disturbances is associated with worse outcomes including increased risk of delirium and cardiac events, and worsened functional recovery. Dexmedetomidine is a highly selective α2-adrenergic agonist with sedative, anxiolytic, and analgesic properties. It exerts sedative effects via activating the endogenous sleep pathways and produces a state like non-rapid eye movement sleep, which is different from opioid- and benzodiazepine-induced sedation. Esketamine is a N-methyl-D-aspartic acid receptor antagonist and has been used as an anesthetic and analgesic. Recent studies showed that low-dose esketamine has anti-depressive and sleep-promoting effects. The investigators suppose that mini-dose dexmedetomidine-esketamine combined infusion at night can improve perioperative sleep quality in patients scheduled for knee or hip replacement surgery.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for phase_4
Started Nov 2023
Typical duration for phase_4
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
July 11, 2023
CompletedFirst Posted
Study publicly available on registry
July 18, 2023
CompletedStudy Start
First participant enrolled
November 1, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2025
CompletedJuly 30, 2025
July 1, 2025
2 years
July 11, 2023
July 29, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Subjective sleep quality in the night of surgery.
Subjective sleep quality will be assessed in the next morning (between 8:00 am to 10:00 am) with the Richards-Campbell Sleep Questionnaire (RCSQ). The RCSQ is a self-reported measure that evaluated perception of nighttime sleep in five items, including sleep depth, sleep latency, number of awakenings, returning to sleep, and overall sleep quality. Each item was assessed with a 100-millimeter visual analog scale (score ranges from 0 to 100, with higher scores representing better sleep). The mean score of the five items represents the overall RCSQ score.
The night on the day of surgery.
Secondary Outcomes (5)
Total sleep time per night during the perioperative period.
From the night before surgery until the second night after surgery.
Sleep efficiency per night during the perioperative period.
From the night before surgery until the second night after surgery.
Sleep onset latency per night during the perioperative period.
From the night before surgery until the second night after surgery.
Wake after sleep onset per night during the perioperative period.
From the night before surgery until the second night after surgery.
Subjective sleep quality during the perioperative period.
From the night before surgery until the fifth night after surgery.
Other Outcomes (9)
Cerebrospinal fluid and blood proteomics examination (selected patients).
During anesthesia.
Intensity of pain during the first 5 postoperative days.
Up to 5 days after surgery.
Use of supplemental analgesics
Up to 5 days after surgery.
- +6 more other outcomes
Study Arms (2)
Dexmedetomidine-esketamine combination
EXPERIMENTALDexmedetomidine-esketamine combination will be infused at a rate of 0.01 ml/kg/h (dexmedetomidine 0.02 μg/kg/h and esketamine 5 μg/kg/h) from 8 pm in the night before surgery until 8 am in the third morning after surgery.
Normal saline
PLACEBO COMPARATORPlacebo (normal saline) will be infused at a rate of 0.01 ml/kg/h from 8 pm in the night before surgery until 8 am in the third morning after surgery.
Interventions
Dexmedetomidine will be infused at a rate of 0.01 ml/ kg/h (0.02 μg/kg/h) from 8 pm in the night before surgery until 8 am in the third morning after surgery.
Esketamine will be infused at a rate of 0.01 ml/ kg/h (5 μg/kg/h) from 8 pm in the night before surgery until 8 am in the third morning after surgery.
Normal saline will be infused at a rate of 0.01 ml/ kg/h from 8 pm in the night before surgery until 8 am in the third morning after surgery.
Eligibility Criteria
You may qualify if:
- Age ≥65 years and \<90 years;
- Scheduled to undergo unilateral knee or hip arthroplasty.
You may not qualify if:
- Refuse to participate;
- Hypnotic therapy for sleep disorders within 3 months;
- Preoperative history of schizophrenia, epilepsy, Parkinson's disease, or myasthenia gravis;
- Diagnosed as obstructive sleep apnea, or at high risk of moderate to severe obstructive sleep apnea according to the Stop-Bang questionnaire;
- Inability to communicate in the preoperative period because of coma, profound dementia, or language barrier;
- Sick sinus syndrome, severe sinus bradycardia (heart rate \<50 beats/min), or atrioventricular block above grade II without pacemaker implanted;
- Severe hepatic dysfunction (Child-Pugh class C), renal dysfunction (required preoperative dialysis), or expected survival ≤24 hours;
- Receiving treatment with dexmedetomidine, clonidine, or esketamine;
- Allergy to dexmedetomidine or esketamine.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Peking University First Hospitallead
- Beijing Hospitalcollaborator
Study Sites (2)
Beijing Hospital
Beijing, Beijing Municipality, 100005, China
Peking University First Hospital
Beijing, Beijing Municipality, 100034, China
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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
- phase 4
- 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
Study Record Dates
First Submitted
July 11, 2023
First Posted
July 18, 2023
Study Start
November 1, 2023
Primary Completion
November 1, 2025
Study Completion
December 1, 2025
Last Updated
July 30, 2025
Record last verified: 2025-07
Data Sharing
- IPD Sharing
- Will not share