None listed
Conditions
Interventions
Sponsors
The First Affiliated Hospital of Zhengzhou University
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. Aged 18-65 years; 2. ASA grade I-III; 3. 20<=BMI < 25kg/m^2; 4. The estimated operation time is 2-6h; 5. Informed consent can be signed.
Exclusion criteria
Exclusion criteria: 1. Received any form of local anesthesia during perioperative period; 2. Patients with expected difficult airway; 3. Combined with central or peripheral nervous system diseases; 4. Baseline SBP 140 mmHg, baseline heart rate 90 bpm; 5. Patients with arrhythmia and pacemaker application; 6. Combined liver and kidney insufficiency; 7. Have used opioids within 30 days; 8. Drug abuse; 9. Suffers from mental illness or is unable to work together; 10. Those who participated in other clinical trials within the past 3 months.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Rifentanil dosage;Opioid dosage 48 hours postoperatively; | — |
Secondary
| Measure | Time frame |
|---|---|
| Numeric rating scale score for pain;Ramsay score;Type, time and dosage of vasoactive drugs;Postoperative recovery room stay time;Bispectral index (BIS) value of EEG;Analgesic index(PTi);Blood pressure;Heart rate;The time between the end of the operation and the time of extubation;Intraoperative hypertension/hypotension events;TacIntraoperative hycardia/bradycardia events;Intraoperative awareness; | — |
Countries
China
Contacts
Public ContactYang Jianjun
Outcome results
None listed