Patients who underwent digestive endoscopic ultrasonography
Conditions
Interventions
Moderate sedation group:Dexmedetomidine was pumped intravenously
Deep sedation group:Propofol was injected intravenously
Sponsors
West China Hospital, Sichuan University
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1. Patients who underwent digestive endoscopic ultrasonography or EUS-FNA; 2. Aged 18 to 60 years, Male or female; 3. ASA level I~II; 4. Body mass index (BMI) 18~30 kg / ?; 5. Willing to sign informed consent and strictly follow the clinical program.
Exclusion criteria
Exclusion criteria: 1. Allergy to propofol, dexmedetomidine, fentanyl and its relief drugs, soy, etc; 2. Had a history of sedation/anesthesia accidents; 3. Severe cardiovascular and cerebrovascular diseases; 4. Severe lung disease; 5. Difficult airway; 6.Sleep apnea syndrome; 7.Pregnant and nursing women; 8. Subjects considered by the investigator to have any other factors not suitable for participation in the clinical study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative comfort of the patient; | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative comfort indexes;Sedation related adverse reactions;Endoscopic physician satisfaction; | — |
Countries
China
Contacts
Public ContactXiao Wang
West China Hospital, Sichuan University
Outcome results
None listed