Gastroenteroscopy anesthesia
Conditions
Interventions
Experimental group:Esketamine + Propofol
Conrol group:Fentanyl + Propofol
Sponsors
West China School of Public Health and West China Fourth Hospital, Sichuan University
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1. The patient was confirmed to be able to participate in painless gastroenteroscopy by the expert consensus opinion on sedation and anesthesia in the diagnosis and treatment of digestive endoscopy in China, which met the relevant standards required for anesthesia; 2. Have basic cognitive awareness, can cooperate with the relevant anesthesia treatment; 3. The functions of heart and lung, liver and kidney were in normal state; 4. Aged 18-60 years; 5. The American Society of Anesthesiologists' classification is grade I or II; 6. Patients and their family members clearly knew the purpose and operation process of the study, and signed the informed letter by the patients themselves, agreeing to participate in the study.
Exclusion criteria
Exclusion criteria: 1. Complicated with severe anemia, acute colitis, congenital gastrointestinal malformation, extensive adhesion in the abdominal cavity and other diseases; 2. Women during menstruation, lactation and pregnancy; 3. Allergic to drugs used in the study: propofol and esketamine; 4. Patients with severe hypertension, coronary heart disease, asthma, systemic infectious diseases, nervous system diseases or medical history; 5. Patients with drug dependence or a history of drug dependence.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| propofol; | — |
Countries
China
Contacts
Public ContactQing Ailing
West China Fourth Hospital, Sichuan University
Outcome results
None listed