visceral pain
Conditions
Interventions
Anxiety group (group A):Sequential experiment: The initial dose of propofol is 3.5 mg/kg. The common dose ratio of propofol for patients is 0.9. If a positive reaction occurs, the next patient will in
Non-anxiety group (group C):Sequential experiment: The initial dose of propofol is 3.5 mg/kg. The common dose ratio of propofol for patients is 0.9. If a positive reaction occurs, the next patient wil
Sponsors
The People's Hospital of Qiannan
Eligibility
Sex/Gender
Female
Age
18 Years to 50 Years
Inclusion criteria
Inclusion criteria: Painless artificial abortion was performed under general anesthesia. The age was 18-50 years old and the body mass index was 18-25 kg / m2 ASA ? ~ ?.
Exclusion criteria
Exclusion criteria: Patients with long-term use of opioids, antianxiety drugs, antidepressants, history of alcohol or drug abuse, neurological or mental illness, and inability to complete the anxiety scale. 30min was evaluated by patients themselves with self-rating anxiety scale (SAS) before operation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Visceral pain; | — |
Secondary
| Measure | Time frame |
|---|---|
| MAP;HR;SPO2;adverse reactions;Agitation during awakening; | — |
Countries
China
Contacts
Public ContactChen Lvlv
The People's Hospital of Qiannan
Outcome results
None listed