PONV
Conditions
Interventions
Control group:tolidansetron
Sponsors
The Second Affiliated Hospital of Nanjing University of Chinese Medicine
Eligibility
Sex/Gender
Female
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1. Female patients, 18-60 years old, BMI 18-22 kg/m2, ASA grade I-II, elective painless gastrointestinal endoscopy; 2. Those who voluntarily join the researcher after informed consent; 3. No history of motion sickness; 4. Those who did not receive antiemetic drugs and opioids within one month before operation.
Exclusion criteria
Exclusion criteria: 1. People suffering from mental illness, cognitive and verbal dysfunction; 2. Patients with a history of PONV; 3. Those who do not accept transcutaneous acupoint electrical stimulation therapy; 4. Severe adverse reactions or other complications occurred during the trial; 5. Anesthesia time >= 1 h.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Substance P;Nausea and vomiting after general anesthesia (PONV);PONV visual analog scoring; | — |
Secondary
| Measure | Time frame |
|---|---|
| Age;Height;Body Mass Index;American Society of Anesthesiologists grading;Apfel Rating;Anesthesia induction;Inspection time;Awakening time;Infusion volume;Non-invasive oxygen saturation;Non-invasive blood pressure;Heart rate;Anesthetic fluid dosage; | — |
Countries
China
Contacts
Public ContactQiu Ying
The Second Affiliated Hospital of Nanjing University of Chinese Medicine
Outcome results
None listed