Dexmedetomidine Clinical Trial
Official title:
Effect of Mini-dose Dexmedetomidine-Esketamine Infusion on Sleep Quality in Older Patients Undergoing Knee or Hip Replacement Surgery: A Multicenter Randomized Controlled Trial
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.
Status | Recruiting |
Enrollment | 154 |
Est. completion date | December 2027 |
Est. primary completion date | December 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 65 Years to 90 Years |
Eligibility | Inclusion Criteria: - Age =65 years and <90 years; - Scheduled to undergo unilateral knee or hip arthroplasty. Exclusion Criteria: - 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. |
Country | Name | City | State |
---|---|---|---|
China | Beijing Hospital | Beijing | Beijing |
China | Peking University First Hospital | Beijing | Beijing |
Lead Sponsor | Collaborator |
---|---|
Peking University First Hospital | Beijing Hospital |
China,
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* Note: There are 41 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Cerebrospinal fluid and blood proteomics examination (selected patients). | Cerebrospinal fluid and blood sample will be collected. Deep proteome analysis will be performed to detect protein biomarkers including amyloid-beta, total tau, and phosphorylated tau. | During anesthesia. | |
Other | Intensity of pain during the first 5 postoperative days. | Intensity of pain will be assessed twice after surgery with the Numeric Rating Scale (an 11- point scale where 0 indicates no pain and 10 the worst pain). | Up to 5 days after surgery. | |
Other | Use of supplemental analgesics | Include opioids and non-opioid analgesics. | Up to 5 days after surgery. | |
Other | The incidence of delirium within 5 days after surgery. | Delirium is assessed twice daily (8:00-10:00 am and 6:00-8:00 pm) with the 3-minute diagnostic interview for Confusion Assessment Method-defined delirium (3D-CAM). | Up to 5 days after surgery. | |
Other | Length of stay in hospital after surgery. | Length of stay in hospital after surgery. | Up to 30 days after surgery. | |
Other | Occurrence of non-delirium complications within 30 days after surgery. | Indicated new-onset conditions other than delirium that required therapeutic intervention within 30 days after surgery. | Up to 30 days after surgery. | |
Other | Subjective sleep quality (Pittsburgh Sleep Quality Index) at 3 months after surgery. | Subjective sleep quality at 30 days after surgery will be assessed with the Pittsburgh Sleep Quality Index. This is a self-rated questionnaire which assesses sleep quality and disturbances over a 1-month time interval. Nineteen individual items generate seven "component" scores: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleeping medication, and daytime dysfunction. The sum of scores for these seven components yields one global score. | At the end of the 3rd month after surgery. | |
Other | Cognitive function at 3 months after surgery. | Cognitive function is assessed with the modified Telephone Interview for Cognitive Status. | At the end of the 3rd month after surgery. | |
Other | Health related quality of life at 3 months after surgery. | Health related quality of life is assessed with the short-form 36-item health survey questionnaire (SF-36). The SF-36 scale measures eight aspects of health status, i.e., physical functioning, role physical, bodily pain, general health, vitality, social functioning, role emotional, and mental health. It also measures changes of subjective healthy status during the last year (reported health transition). The scores of the above 9 items are calculated separately with scores range from 0 to 100, with higher score indicating better quality. | At the end of the 3rd month after surgery. | |
Primary | 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 | Total sleep time per night during the perioperative period. | Objective sleep quality will be monitored with the SOMNOtouch NIBP (Somnomedics GmbH, Randersacker, Germany) from 8:00 pm to 8:00 am from the night before surgery until the fifth night after surgery. Total sleep time is defined as the sum in time scored as asleep. | From the night before surgery until the second night after surgery. | |
Secondary | Sleep efficiency per night during the perioperative period. | Objective sleep quality will be monitored with SOMNOtouch NIBP (Somnomedics GmbH, Randersacker, Germany) from 8:00 pm to 8:00 am from the night before surgery until the fifth night after surgery. Sleep efficiency is defined as the ratio of total sleep time/time in bed. | From the night before surgery until the second night after surgery. | |
Secondary | Sleep onset latency per night during the perioperative period. | Objective sleep quality will be monitored with SOMNOtouch NIBP (Somnomedics GmbH, Randersacker, Germany) from 8:00 pm to 8:00 am from the night before surgery until the fifth night after surgery. Sleep onset latency is defined as time difference between time to bed and sleep start. | From the night before surgery until the second night after surgery. | |
Secondary | Wake after sleep onset per night during the perioperative period. | Objective sleep quality will be monitored with SOMNOtouch NIBP (Somnomedics GmbH, Randersacker, Germany) from 8:00 pm to 8:00 am from the night before surgery until the fifth night after surgery. Wake after sleep onset is defined as the total time scored as awake between sleep start and sleep end. | From the night before surgery until the second night after surgery. | |
Secondary | Subjective sleep quality during the perioperative period. | Subjective sleep quality will be assessed daily in the next morning (between 8:00 am to 10:00 am) using the Richards-Campbell Sleep Questionnaire (RCSQ). | From the night before surgery until the fifth night after surgery. |
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