None
Conditions
Interventions
Test team A:Lidocaine 1mg/kg , analgesic 8 µg/kg, propofol 1.5-2.5mg/kg were administered intravenously.
Test team B:Lidocaine was given intravenously at 1.5mg/kg (up to 100mg), analgesic at 8 µg/kg, and propofol at 1.5-2.5mg/kg.
Control group C:Equal amounts of normal saline were given instead of intravenous lidocaine, and alfentanil 8 µg/kg was administered. Propofol: 1.5-2.5 mg/kg.
Sponsors
The First Affiliated Hospital of Baotou Medical College
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1) Age: 18-60 years old, ASA grade I-II. 2) Scheduled for elective painless gastroscopy (gastroscopy + colonoscopy). 3) Sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1) Allergy to the test drug. 2) Severe cardiopulmonary disease (such as uncontrolled hypertension, asthma, COPD). 3) Pregnant or lactating women. 4) Long-term use of analgesic/ sedative drugs.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Anesthetic effects (induction time, recovery time);The amount of propofol used;Hemodynamic parameters (heart rate, blood pressure, oxygen saturation, etc.);Untoward effect( respiratory depression, injection pain, hypotension); | — |
Secondary
| Measure | Time frame |
|---|---|
| Patient satisfaction score;Postoperative recovery quality; | — |
Countries
China
Contacts
Public ContactQi Fengling
The First Affiliated Hospital of Baotou Medical College
Outcome results
None listed