Obesity
Conditions
Interventions
Experimental group:Sedation: Rimazolen intravenous sedation
Sponsors
Jiangsu Integrated Traditional Chinese and Western Medicine Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. Age range: 18-65 years old, planned to undergo painless gastroscopy (colonoscopy) 2. Body Mass Index (BMI >=30kg/m^2) 3. No symptoms of upper respiratory tract infection in the past two weeks 4. American Society of Anesthesiologists (ASA) classification: Grade I/II/III
Exclusion criteria
Exclusion criteria: 1. Patients who did not sign the informed consent form for clinical trials and refused to participate in this study 2. Previous history of allergies to any medication required in the study 3. Patients with mental or communication disorders who are unable to cooperate in collecting information 4. ASA >= IV or severe unstable systemic diseases (such as uncontrolled heart failure, respiratory failure) 5. Patients with long-term heavy use of opioids/sedatives 6. Researchers believe that patients who are not suitable to participate in the experiment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of hypoxemia; | — |
Secondary
| Measure | Time frame |
|---|---|
| Incidence of moderate hypoxemia;Incidence of severe hypoxemia;Airway intervention needs;Success rate of conscious sedation;Endoscope satisfaction score;Patient satisfaction rating;Anesthesia related adverse reactions; | — |
Countries
China
Contacts
Public ContactHe Rong
Jiangsu Integrated Traditional Chinese and Western Medicine Hospital
Outcome results
None listed