Painless gastrointestinal endoscopy
Conditions
Interventions
Control group:administrating 2ml NS
Experimental group:administrating 0.01mg/kg atropine(2ml)
Sponsors
The 2nd Affiliated Hospital of Wenzhou Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. undergoing gastrointestinal endoscopy; 2. Aged 18-65 years old; 3. ASAI-II; 4. BMI 18 to 26kg/m2; 5. obtain written informed consent; 6. Diagnosted by the same endoscopist.
Exclusion criteria
Exclusion criteria: 1. To be allergic to propofol; 2. have ever suffered from glaucoma or prostatomegaly; 3. suffered from diabetes and hyperthyreosis; 4. tachycardia and other arrhythmia; 5. have ever suffered from abdominal operation; 6. liver and kidney dysfunctionl; 7. plan to be conducted endoscopic treatment.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| D-value of MAP between baseline and the messureing time point;D-value of MAP between baseline and the messureing time point;D-value of MAP between baseline and the messureing time point;D-value of MAP between baseline and the messureing time point;D-value of MAP between baseline and the messureing time point;The duration of gastroscopy;The duration of colonoscopy; | — |
Secondary
| Measure | Time frame |
|---|---|
| the satisfaction degree of endoscopist;the satisfaction degree of patients;the incidence of xerostomia;The total using dose of propofol; | — |
Countries
China
Contacts
Public ContactRuifeng Zeng
Department of Anesthesiology, The 2nd Affiliated Hospital of Wenzhou Medical University
Outcome results
None listed