pain
Conditions
Interventions
experimental group:Propofol/Esketamine
control group:Propofol/Fentanyl
Sponsors
Tianjin Union Medical Center
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: 1. Subject's American Society of Anesthesiologists physical status is I-III. 2. Subject has no symptoms of allergy to anesthetics. 3. Subject has no contraindications for gastrointestinal endoscopy. 4. Subject has given written informed consent to participate.
Exclusion criteria
Exclusion criteria: 1. Subject's BMI 30; 2. Subject has poorly controlled or untreated hypertension; 3. Subject has severe ischemic heart disease; 4. Subject is an untreated or undertreated patient with hyperthyroidism; 5. Subject has used drugs that affect their central nervous system; 6. Subject has mental illness; 7. Subject has epilepsy; 8. Subject has a history of chronic pain; 9. Subject is pregnant or breast-feeding.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cumulative propofol Consumption; | — |
Secondary
| Measure | Time frame |
|---|---|
| The incidence of adverse events in pulmonary and circulatory systems;The Times of the patients motion reaction during operation;The satisfaction of the endoscopist and patient;Time of recovery, PACU and discharge from hospital; | — |
Countries
China
Contacts
Public ContactYang Tao
Tianjin Union Medical Center
Outcome results
None listed