Postoperative sleep disorders
Conditions
Interventions
Propofol sedation group:NA
Control group:NA
Sponsors
Tongde Hospital of Zhejiang Province
Eligibility
Sex/Gender
Female
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: 1. Women aged 18-45 years; 2. American Society of Anesthesiologists (ASA) physical status I – III; 3. Patients undergoing eElective cesarean section with spinal anesthesia; 4 .Patients verbally agreed to participate in this study;
Exclusion criteria
Exclusion criteria: 1. Patients who received other intravenous anesthetics except propofol after extraction of the fetus; 2. Failure of spinal anesthesia; 3. Chronic life-threatening comorbidities (e.g. chronic obstructive pulmonary disease, pulmonary hypertension, or a history of congestive heart failure); 4. Severe mental disorder; 5. Long-term use of hypnotics and sedatives; 6. Inability to communication; 7. Patients who refused to participate.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sleep quality; | — |
Secondary
| Measure | Time frame |
|---|---|
| Depression; | — |
Countries
China
Contacts
Public ContactJie Zhou
Tongde Hospital of Zhejiang Province
Outcome results
None listed