Cervical cancer, cervical neoplasia
Conditions
Interventions
Test group: ultrasound-guided sacral block group:Ultrasound-guided sacral block
Control group: subarachnoid space block group:Subarachnoid space block
Sponsors
The first affiliated hostipal of nanchang university
Eligibility
Sex/Gender
Female
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. Before the trial, understand the nature, significance, possible benefits, possible inconveniences and potential risks of the trial in detail, understand the study procedures and sign the informed consent form; 2. Patients undergoing cervical conization were treated by the same group of doctors; 3. sex, aged 18-65 years; 4. weight >= 45kg, BMI 19.0~26.0kg/m^2; 5. ASA of anesthesia is grade I~II;
Exclusion criteria
Exclusion criteria: 1. allergy to local anesthetics; 2. mental problems; 3. emergent disease; 4. systemic anticoagulation; 5. peripheral neuropathy; 6. injection site infection; 7. Diabetes;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Qor-15 score; | — |
Secondary
| Measure | Time frame |
|---|---|
| NRS pain score;Postoperative nausea and vomiting incidence;Incidence of transient neurological syndrome;Total consumption of intravenous drugs within 24h;Time required for analgesia;Flurfenoxil consumption within 24 hours;Occurrence of intraoperative hypotension;Patient perioperative satisfaction;Intraoperative use of pressor drugs;Satisfaction with anesthesia by itinerant nurses;;Intestinal function recovery time;Surgeons 'satisfaction with surgical conditions;Time to get out of bed; | — |
Countries
China
Contacts
Public ContactYang Zhang
The first affiliated hostipal of nanchang university
Outcome results
None listed