postoperative cognitive dysfunction
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) undergoing elective lower limb long bone surgery (the operation time was 3-4 hours); (2) age =65 years old; (3) ASA?/?, MMSE score =23; (4) those who voluntarily participated in the study and signed the informed consent form
Exclusion criteria
Exclusion criteria: (1) known to be allergic to the components of the investigational drug; (2) inability to cooperate, such as mental disorders or anticipated difficulties with neuropsychological assessment, communication difficulties related to pronunciation or dialect. (3) those with a history of alcohol or drug abuse; (4) participants who were enrolled in or had enrolled in another clinical trial within 12 weeks before the trial; (5) Other patients who, in the judgment of the investigator, would not be eligible to participate in the trial, such as acute or chronic infectious diseases, secondary surgery, ASA score greater than grade III, illiteration, stroke or transient ischemic attack within 1 month.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of postoperative cognitive impairment; | — |
Secondary
| Measure | Time frame |
|---|---|
| The use of analgesic drugs in patients;Patient's pain level;The mean arterial pressure of the patients during the procedure;Adverse reactions within 24 hours after operation were recorded;Length OF STAY;Continuous pulse oxygen saturation was measured 24 hours after surgery;The first postoperative defecation time;The first time of ground movement; | — |
Countries
China
Contacts
Hospital of Traditional Chinese Medicine Affiliated to Southwest Medical University