None listed
Conditions
Interventions
propofol group:Propofol induced and maintained anesthesia
Remazolam group:Remazolam induced and maintained anesthesia
cipofol group:cipofol induced and maintained anesthesia
Sponsors
Deyang People's Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. Patients with ASA grading I-II and scheduled painless gastroscopy, colonoscopy, and gastroscopy; 2. Respiratory rate 12-18 beats/min, heart rate 50-100 beats/min, systolic blood pressure>=90 mmHg, diastolic blood pressure>=60 mmHg, SpO2>95% when inhaling air; 3. Able to understand the research process and effectively communicate with researchers; 4. Voluntarily participate and sign an informed consent form.
Exclusion criteria
Exclusion criteria: 1. Allergies to the following drugs or drug adjuvants: opioids, benzodiazepines, flumazenib, propofol or cyclophenol and their adjuvants (soybean oil, glycerol, triglycerides, lecithin, sodium oleate, sodium hydroxide); 2. Have contraindications to deep sedation or anesthesia, or have a history of adverse reactions to sedation or anesthesia; 3. Have used opioid analgesics and benzodiazepine sedative hypnotics within one month; 4. Within 3 months of becoming addicted to drugs or participating in other clinical trials, or drinking more than 14 units of alcohol per week (1 unit=360 mL of beer or 45 mL of 40% alcohol or 150 mL of wine); 5. Difficult airway: Mallampati grading>=3 grades; 6. Pregnant or lactating women; 7. Serious psychological disorders, emotional disorders, and other factors that researchers consider unsuitable for inclusion in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| incidence of dreaming;type of dream; | — |
Secondary
| Measure | Time frame |
|---|---|
| evaluation ;improvement of the sleep quality;incidence of insufficient anesthesia;incidence of intraoperative awareness; | — |
Countries
China
Contacts
Public ContactXia Leqiang
Deyang People's hospital
Outcome results
None listed