Abdominal pain
Conditions
Interventions
Fospropofol Disodium Group:Sedation with fospropofol disodium
Propofol Group:Propofol sedation
Sponsors
The People's Hospital of Fengqing
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. Age >=18 years old, < 65 years old; 2.BMI: 18-28 kg/m ²; 3.ASA classification I- II;
Exclusion criteria
Exclusion criteria: 1. Refuse to participate; 2. Severe diseases of vital organs such as the heart, liver, kidneys and lungs; 3. Allergic to benzodiazepines and long-term use of benzodiazepines; 4. Pregnant or lactating patients; 5. History of drug abuse or alcoholism; 6. There is a history of abnormal recovery from anesthesia and allergy to anesthetic drugs in the past; 7. Improve the Mallampati classification to level IV; 8. Other reasons why the researcher deems the patient unsuitable to participate in this study must be clearly and detailly recorded in the CRF.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Success rate of induction and sedation; | — |
Secondary
| Measure | Time frame |
|---|---|
| Additional Drug Administration Status;Satisfaction;Induction time;Emergence time;PACU stay time;Total Dosage of Fospropofol Disodium and Propofol;Vital Signs; | — |
Countries
China
Contacts
Public ContactWangYanli
The People's Hospital of Fengqing
Outcome results
None listed