None listed
Conditions
Interventions
Control Group:fentanil+propoful
Experimental Group:afentanil+propofol
Sponsors
Yan'an Branch of Perking University Third Hospital (Yan'an City Hospital of TCM)
Eligibility
Sex/Gender
All
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1. Aged >=18 years; 2. ASA grading ?-?; 3. Body Mass index (BMI) 17-24 kg/m^2.
Exclusion criteria
Exclusion criteria: 1. Patients or family members refuse to participate; 2. Severe insufficiency of heart, lung, brain and other important organs; 3. Difficult airway; 4. History of alcohol abuse; 5. Difficulty in communication or cooperation; 6. Allergic to the drugs used; 7. Gastrointestinal bleeding; 8. Sedatives, analgesics and monoamine oxidase inhibitors have been used recently.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| awake time;intraoperative consumption of propofol;incidence of choking;incidence of propofol injection pain;incidence of body movement;incidence of postoperative nausea and vomiting;incidence of postoperative adverse reactions ; | — |
Secondary
| Measure | Time frame |
|---|---|
| postoperative pain;mean arterial pressure;heart rate; | — |
Countries
China
Contacts
Public ContactZhao Huiling
Yan'an Branch of Perking University Third Hospital (Yan'an City Hospital of TCM)
Outcome results
None listed