Total Laparoscopic Hysterectomy
Conditions
Interventions
Experimental group1:Patients receive total intravenous anesthesia
Experimental group2:patients receive erector spinae plane block
Experimental group3:Patients receive quadratus lumborum block
Sponsors
The Second Affiliated Hospital of Anhui Medical University
Eligibility
Sex/Gender
Female
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. Patients undergoing elective total laparoscopic hysterectomy; 2. Aged 18 to 65 years; 3. ASA Class i–ii.
Exclusion criteria
Exclusion criteria: 1. BMI >35kg/?; 2. Those who are allergic to drugs; 3. Patients with abnormal coagulation function; 4. Infection near the puncture; 5. Patients with nervous system and sperm disorders; 6. Severe heart, lung, liver and kidney system insufficiency; 7. Patients with communication barriers or other reasons not applicable to this study were excluded; 8. Those who have a history of chronic pain or who have recently taken analgesic drugs.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| sufentanil consumption in the first postoperative 12h; | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain score of incisional, visceral, shoulder and perineum during the first postoperative 24h;sufentanil consumption during the first postoperative 24h;first time of pressing the PCA pump;pain score of postoperative 3rd and 6th month;duration of anesthesia;duration of surgery;recovery time;first postoperative ambulation time;first postoperative exhaust time;postoperative hospital-stay time;intraoperative sufentanil consumption;intraoperative propofol consumption;intraoperative remifentanil consumption;incidence of adverse event; | — |
Countries
China
Contacts
Public ContactWu Yun
The Second Affiliated Hospital of Anhui Medical University
Outcome results
None listed