Rapid recovery of patients undergoing laparoscopic surgery
Conditions
Interventions
group A:Bilateral ibSLN block (2% lidocaine 3ml) + TAP block, sufentanil induction dose of 0.4ug/kg
group B:Bilateral ibSLN block (2% lidocaine 3ml) + TAP block, sufentanil induction dose of 0.2ug/kg
group C:Bilateral ibSLN block (2% lidocaine 3ml) + TAP block, sufentanil induction dose of 0ug/kg
group D:Bilateral ibSLN block (Physiological saline 3ml) + TAP block, sufentanil induction dose of 0.4ug/kg
Sponsors
Affiliated Hospital of Guilin Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1.Patients scheduled for laparoscopic surgery; 2.American Society of Anesthesiologist's (ASA) grade I to III; 3.Age 18-65 years old, height 145-185cm, weight 45-80kg; 4.Educational level above primary school; 5.Sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1.Participated in other clinical trials within 4 weeks before operation; 2.There are serious heart, lung, liver, kidney and other organ dysfunction; 3.History of neurological and mental illness, long-term use of sedative drugs; 4.Patients have severe aphasia, visual and hearing impairment, severe motor impairment, and are unable to cooperate with the examination; 5.Pregnant or lactating women; 6.Patients with motion sickness and allergy to ropivacaine; 7.The amount of intraoperative blood loss is greater than that of 500ml; 8.Enlarge surgical incision during operation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Usage of sufentanil;Usage of remifentanil;SPO2;heart rate;Blood pressure; | — |
Secondary
| Measure | Time frame |
|---|---|
| Anesthesia time;Blood pressure;Sore throat;imes of nausea and vomiting;NRS pain score at 3, 6, 12, 24 and 48 hours after operation;Types and doses of analgesics used in wards;Other special circumstances; | — |
Countries
China
Contacts
Public ContactZhang Xu
Affiliated Hospital of Guilin Medical University
Outcome results
None listed