Painless gastroscopy
Conditions
Interventions
Trial group:Sufentanil at a dose of 0.1 µg/kg was intravenously injected, followed by intravenous induction of propofol at a dose of 2 mg/kg. During the operation, propofol was pumped at a dose of 2-4
Control group:Oxelidine was intravenously injected at a dose of 0.02 mg/kg, followed by intravenous induction of propofol at a dose of 2 mg/kg. During the operation, propofol was pumped at a dose of 2
Sponsors
Guangzhou Women and Children's Medical Center Liuzhou Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1. Patients who underwent painless gastroscopy at Liuzhou Hospital of Guangzhou Women and Children's Medical Center and voluntarily participated in the study and signed the informed consent form; 2. aged >=18 and <=60 years; 3. BMI 18-28 kg/m^2; 4. ASA classification I or II
Exclusion criteria
Exclusion criteria: 1. Those who have had cognitive dysfunction, suffer from mental disorders, and have communication and interaction difficulties; 2. Those with a history of alcohol or drug abuse; 3. Those who used anesthetic drugs, sedatives, or opioid drugs within 24 hours before the surgery; 4. Those who participated as subjects in any clinical trial within the previous 3 months; 5. Those who are allergic or hypersensitive to the drugs used in this study; 6. Pregnant or lactating women or those with a fertility plan within 3 months; 7. Those with symptoms of acute upper gastrointestinal bleeding or those requiring endoscopic examination and treatment; 8. Those who need complex endoscopic techniques for diagnosis and treatment; 9. Those who plan to undergo tracheal intubation; 10. Those who are judged to have difficult respiratory management.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The incidence of intraoperative respiratory depression; | — |
Secondary
| Measure | Time frame |
|---|---|
| Blood pressure change;heart rate variation;Drug dosage;Awakening time;The sedation level of the patient every 5 minutes within 20 minutes after drug withdrawal; | — |
Countries
China
Contacts
Public ContactOu Lianchun
Guangzhou Women and Children's Medical Center Liuzhou Hospital
Outcome results
None listed