Cervical Intraepithelial Neoplasia
Conditions
Interventions
Group 1:LMA Inhalation anesthesia
Group 2:Spinal anesthesia
Sponsors
Department of anesthesiology, the Second Affiliated Hospital of the Army Medical University
Eligibility
Sex/Gender
Female
Age
20 Years to 40 Years
Inclusion criteria
Inclusion criteria: 1) Aged 20 to 40 years; 2) BMI 18 to 30; 3)ASAI-II; 4) willing to participate in this study and signed informed consent.
Exclusion criteria
Exclusion criteria: 1) a history of drug use, alcohol or opioid abuse; 2) drug allergy or contraindication; 3) pregnant women; 4) patients with serious diseases such as heart, brain, lung, liver, kidney and hematopoietic system; 5) patients with coagulation dysfunction; 6) patients with intra-spinal anesthesia contraindication; 7) patients with laryngeal mask airway ventilation; 8) failure to cooperate with the study for any reason; 9) participated in other clinical trials in March before being included in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| quality of recovery 15; | — |
Secondary
| Measure | Time frame |
|---|---|
| Visceral pain numerical rating scale;Visceral pain numerical rating scale;Visceral pain numerical rating scale;Time to get out of bed for the first time;First feeding time;Postoperative satisfaction survey;Headache and low back pain;Headache and low back pain;Headache and low back pain; | — |
Countries
China
Contacts
Public ContactHong LI
The Second Affiliated Hospital of the Army Medical University
Outcome results
None listed