gastric disease
Conditions
Interventions
Propofol group:Propofol
Sponsors
The Affiliated Hospital of Guizhou Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1.ASA grade I-II; 2.Patients aged 18-65 years old who underwent selective cgastroscopy under general anesthesia; 3.BMI 18-30kg/m2; 4.Sign informed consent.
Exclusion criteria
Exclusion criteria: (1)Those who are allergic or contraindicated to the use of drugs in this study, such as opioids, propofol, ciprofol and their components; (2) Patients with severe sleep disorders; (3) With a history of cognitive dysfunction or inability to communicate; (4) Patients who need advanced therapeutic endoscopy or are expected to take a long time (more than 30min) (5) Patients with a history of any neuropsychiatric disorders, such as depression (6) Abuse of alcohol,benzodiazepines,opioids or other drugs; (7) severe Liver and kidney insufficiency;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Morphine-Benzedrine Group (MBG) score; | — |
Secondary
| Measure | Time frame |
|---|---|
| modified Brice questionnaire;five-point Likert scale;Anxiety and Depression Scale;Preoperative Dream Score;numeric rating scale;Pittsburgh Sleep Quality Index scores;Hall and Van der Castle emotion scale;Patient satisfaction; | — |
Countries
China
Contacts
Public ContactXiaohua Zou
The Affiliated Hospital of Guizhou Medical University
Outcome results
None listed