Painless Gastroscopy
Conditions
Interventions
Group E:propofol+esketamine
Group N:prppofol+0.9% saline
Sponsors
The First Affiliated Hospital of Shantou University Medical College
Eligibility
Sex/Gender
All
Age
18 Years to 64 Years
Inclusion criteria
Inclusion criteria: ASA I-III patients aged 18-64 years, BMI <= 30kg / m2, scheduled to undergo painless gastroscopy in the First Affiliated Hospital of Medical College of Shantou University.
Exclusion criteria
Exclusion criteria: 1. Subjects with allergic history of ketamine, propofol or albumin; 2. Subjects with severe heart, liver and kidney dysfunction; 3. Patients with severe arrhythmia and atrioventricular block; 4. Subjects with psychological problems or history of mental illness or central nervous system problems; 5. Patients treated with sedative hypnotics and / or analgesics for more than 3 months; 6. Patients with serious risk of elevated blood pressure, intracranial pressure and glaucoma; 7. Patients with hyperthyroidism who are under treated or untreated; 8. Patients who refuse to sign informed consent.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The total amount of propofol; | — |
Secondary
| Measure | Time frame |
|---|---|
| Vital signs at different timepoints;intraoperative adverse events;postoperative adverse events;Satisfaction scores of patients;recovery time; | — |
Countries
China
Contacts
Public ContactShaohui Zhuang
The First Affiliated Hospital of Medical College of Shantou University
Outcome results
None listed