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Ameliorative effect of dexmetomidine on postoperative delirium in elderly patients with weakness

Ameliorative effect of dexmetomidine on postoperative delirium in elderly patients with weakness

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200055791
Enrollment
Unknown
Registered
2022-01-19
Start date
2022-06-01
Completion date
Unknown
Last updated
2023-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Delirium

Interventions

control group:Saline was given during the perioperative period.
Low dose group in prophase of weakness (L1 group):A loading dose of Dexametholidine (1mg/kg, within 10min) was pumped intravenously starting 10min before induction of anesthesia, and then a maintenanc
Low dose group in weakness (L2 group):A loading dose of Dexametholidine (1mg/kg, within 10min) was pumped intravenously starting 10min before induction of anesthesia, and then a maintenance dose of 0.
High dose group in prophase of weakness (H1 group) :A loading dose of Dexametholidine (1mg/kg, within 10min) was pumped intravenously starting 10min before induction of anesthesia, and then a maintena
High dose group in weakness (H2 group):A loading dose of Dexametholidine (1mg/kg, within 10min) was pumped intravenously starting 10min before induction of anesthesia, and then a maintenance dose of 0

Sponsors

The Third Medical Center of Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Elderly patients who underwent limb surgery under general anesthesia in our hospital; 2. Aged 60 years or over, regardless of sex; 3. ASA grade: I- III.

Exclusion criteria

Exclusion criteria: 1. Those who had dementia or a clear history of cognitive dysfunction, mental system disease, brain trauma, hearing, vision or language communication disorders could not complete this survey; 2. Patients with delirium were assessed as delirium before operation; 3. Emergency operation; 4. Patient or the guardian did not sign the informed consent form; 5. Major complications occurred during and after operation, such as cardiac arrest, pulmonary embolism and so on.

Design outcomes

Primary

MeasureTime frame
POD;

Secondary

MeasureTime frame
Arterial blood S100 ß;Interleukin 1 ß;

Countries

China

Contacts

Public ContactLiu Yongzhe

Anesthesia Department of the Third Medical Center of PLA General Hospital

lyzgao@163.com+86 15811331366

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026