Bariatric surgery
Conditions
Interventions
control group:Maintenance with propofol
experimental group:Maintenance with isoflurane
Sponsors
The First Affiliated Hospital of the Air Force Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1) Adult patients undergoing laparoscopic bariatric surgery; 2) ASA physical status I–III; 3) Patients who voluntarily participated in the study and signed informed consent.
Exclusion criteria
Exclusion criteria: 1) Age < 18; 2) Severe cardiopulmonary disease or severe organ function instability; 3) Patients who plan to enter ICU after operation; 4) Mental Disorders affecting cognition, judgment and compliance; 5) Pregnancy,drug abuse, alcohol dependence; 6) Patients have history of drug allergy; 7) Patients participating in other clinical trials.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Recovery quality after anesthesia; | — |
Secondary
| Measure | Time frame |
|---|---|
| Incidence of perioperative hypoxemia;time to awakening;quality assessment of wakefulness;Postoperative pain assessment;Postoperative nausea assessment;Incidence of postoperative vomiting;hospital length of stay; | — |
Countries
China
Contacts
Public ContactZhenghua Zhu
Outcome results
None listed