Gastrointestinal disease
Conditions
Interventions
group PD :Propofol combined with dexmedetomidine
group PR :Propofol combined with remifentanil
Sponsors
Affiliated Cancer Hospital of Shandong First Medical University, Shandong Cancer Institute
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: Patients aged 18–75 years, with ASA (American Society of Anesthesiology) I–III, and scheduled for painless endoscopic ultrasonography.
Exclusion criteria
Exclusion criteria: 1. BMI>25 kg/m^2 or < 18 kg/m^2; 2. Pregnancy; 3. There are serious complications (such as: heart failure, respiratory failure, liver or kidney failure), heart conduction disease bradycardia, or abnormal rhythm; 4. History of asthma or chronic bronchitis, upper respiratory tract infection within the past 2 weeks, obstructive sleep apnea; 5. Allergic to the drugs used in the research; 6. History of drug abuse.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| endoscopy physician satisfaction; | — |
Secondary
| Measure | Time frame |
|---|---|
| patient satisfaction;induction time;time of reached the standard for discharge;body movement;cardiopulmonary adverse event; | — |
Countries
China
Contacts
Public ContactWang Xiuqin
Affiliated Cancer Hospital of Shandong First Medical University, Shandong Cancer Institute
Outcome results
None listed