NCT05950646

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

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
154

participants targeted

Target at P50-P75 for phase_4

Timeline
Completed

Started Nov 2023

Typical duration for phase_4

Geographic Reach
1 country

2 active sites

Status
recruiting

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

Completed
7 days until next milestone

First Posted

Study publicly available on registry

July 18, 2023

Completed
4 months until next milestone

Study Start

First participant enrolled

November 1, 2023

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2025

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2025

Completed
Last Updated

July 30, 2025

Status Verified

July 1, 2025

Enrollment Period

2 years

First QC Date

July 11, 2023

Last Update Submit

July 29, 2025

Conditions

Keywords

Old AgeKnee Replacement SurgeryHip Replacement SurgeryDexmedetomidineEsketamineSleep Quality

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

EXPERIMENTAL

Dexmedetomidine-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.

Drug: DexmedetomidineDrug: Esketamine

Normal saline

PLACEBO COMPARATOR

Placebo (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.

Drug: Normal saline

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.

Dexmedetomidine-esketamine combination

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.

Dexmedetomidine-esketamine combination

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.

Normal saline

Eligibility Criteria

Age65 Years - 90 Years
Sexall
Healthy VolunteersNo
Age GroupsOlder Adult (65+)

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

Study Sites (2)

Beijing Hospital

Beijing, Beijing Municipality, 100005, China

RECRUITING

Peking University First Hospital

Beijing, Beijing Municipality, 100034, China

RECRUITING

Related Publications (41)

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MeSH Terms

Conditions

Sleep Initiation and Maintenance Disorders

Interventions

DexmedetomidineEsketamineSaline Solution

Condition Hierarchy (Ancestors)

Sleep Disorders, IntrinsicDyssomniasSleep Wake DisordersNervous System DiseasesMental Disorders

Intervention Hierarchy (Ancestors)

ImidazolesAzolesHeterocyclic Compounds, 1-RingHeterocyclic CompoundsCrystalloid SolutionsIsotonic SolutionsSolutionsPharmaceutical Preparations

Study Officials

  • Dong-Xin Wang, MD,PhD

    Peking University First Hospital

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Dong-Xin Wang, MD,PhD

CONTACT

Shuang-Jie Cao, MD

CONTACT

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

Locations