Intranasal Insulin Improves Postoperative Neurocognitive Disorders in Elderly Patients
Postoperative Neurocognitive Disorders
About this trial
This is an interventional health services research trial for Postoperative Neurocognitive Disorders focused on measuring postoperative neurocognitive disorders, Intranasal insulin
Eligibility Criteria
Inclusion Criteria: Patients under general anesthesia through oral intubation; Patients undergoing elective extrathoracic, breast, orthopaedic, urological, abdominal and gynecological operations; Age ≥ 65 years; Cardiac function grade I~II (NYHA standard), ASA grade I~III; Volunteer for anticipating study and sign an informed consent form; Exclusion Criteria: Diabetes patients; Previous history of craniocerebral and spinal cord trauma, surgery, stroke, and inability to place electrodes on the head; History of nasal cavity stuffiness, epistaxis, rhinitis, and nasopharynx surgery; The operation position is prone and it is difficult to implement intranasal administration; Those who cannot cooperate with the assessment of the scale or have delirium before operation; Preoperative fasting blood glucose<4 mmol/L; Those who have participated in other clinical trials.
Sites / Locations
- First Affiliated Hospital of Xian Jiaotong UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
Intranasal insulin group
Saline group
Before anesthesia induction, give the first insulin nasal spray, once per hour, 20 IU each time, until the end of the operation
Before anesthesia induction, give the equal volumes'saline nasal spray, once per hour, 20 IU each time, until the end of the operation