postoperative sleep disturbance
Conditions
Interventions
B Group:DEX+ Pseudo TEAS
C Group:TEAS + NS
D Group:Pseudo TEAS + NS
A group:Dexmedetomidine (DEX) and transcutanclus electrical acupoint stimulation (TEAS)
Sponsors
the First People's Hospital of Changde
Eligibility
Sex/Gender
Female
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: (1) Voluntarily participate in this study, have full capacity for civil conduct, and sign informed consent. (2) Patients undergoing elective gynecological laparoscopic surgery , aged 18 to 65 years, BMI of 18.5 to 30 kg/m2, ASA grade I to ?, expected operation duration of more than 1 hour. (3) The patient did not participate in other drug clinical trials nearly 3 months before enrollment.
Exclusion criteria
Exclusion criteria: (1) Refuse to participate in the study; (2) preoperative sleep disturbance, PSQI=7 points; (3) Both cardiac pacemaker implantation; Taking anticoagulant after the operation of large heart vessels; (4) suffering from other endocrine and metabolic diseases; (5) A history of serious chronic diseases of the heart, brain, lung, liver, kidney, etc.; (6) Local skin allergy, damage or infection at the acupoint selection site; Suffering from a mental disorder, depression or neurological disease; (7) Taking drugs related to sleep before surgery; (8) Difficulty in communication; Unable to cooperate with the completion of relevant scale measurement; Severe hearing or visual impairment, unable to communicate effectively; (9) Pathological sinus syndrome, severe sinus bradycardia (<50/min), or secondary or higher atrioventricular block without pacemaker; (10) Allergies to opioid analgesics or DEX.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| ncidence of postoperative sleep disturbance; | — |
Secondary
| Measure | Time frame |
|---|---|
| SMH scores;NRS pain scores;PSQI score;SMH score; | — |
Countries
China
Contacts
Public ContactLiu Hongbo
the First People's Hospital of Changde
Outcome results
None listed