Sleep disorder
Conditions
Interventions
MD Group (Composite Dextromet Group):Dextromet low-dose nasal spray was given on the evening before surgery and the evening after surgery, and intraoperative dextromet was pumped intravenously to prev
SD Group (Single Species Right American Group): intraoperative dextromet was pumped intravenously to prevent sleep disorders only
Group C (Control group):Administer physiological saline solution
Sponsors
Maternal and Child Health Hospital of Linping District, Hangzhou
Eligibility
Sex/Gender
Female
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Age 18-60 years, American Society of Anesthesiologists (ASA) class I-III, no history of psychiatric illness, no other medical studies.
Exclusion criteria
Exclusion criteria: (1) Preoperative Pittsburgh Sleep Quality Index (PSQI) >= 7 or Athens Insomnia Scale (AIS) >= 6; (2) Sleep apnea or moderate or severe snoring; (3) Implantation of an in situ pacemaker, preoperative sinus bradycardia (heart rate < 50 beats/min) or sinus node disease, second or third degree atrioventricular block; (4) Preoperative communication disorders; (5) Severe liver or renal insufficiency; (6) Preoperative anti-epileptic, antidepressant and other psychotropic drugs; (7) Serious surgery-related adverse reactions and complications during the perioperative period.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| sleep quality; | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative pain, nausea and vomiting;Pain score;Adverse reactions; | — |
Countries
China
Contacts
Public ContactSufeng Lin
Linping District Women and Children Care Hospital, Hangzhou
Outcome results
None listed