acute postoperative pain
Conditions
Interventions
sufentanil+sufentanil group:sufentanil iv. injection+sufentanil PCIA
oxycodone+oxycodone group:oxycodone iv. injection+oxycodone bolus only PCIA
sufentanil+oxycodone group:sufentanil iv. injection+oxycodone bolus only PCIA
oxycodone+sufentanil group:oxycodone iv. injection+sufentanil PCIA
Sponsors
Shaanxi province tumor hospital
Eligibility
Sex/Gender
Female
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Adults patients undergoing selective gynecological tumors surgery were included. Patients aged 18-6 year-old, BMI 18-29.5, ASA I-III
Exclusion criteria
Exclusion criteria: Patients with cardiac, pulmonary, hepatic or renal insufficiency, drug history including opioid analgesics, NSAIDs, sedative and antidepressant more than 1 month, alcohol abuse history, having mental diseases, sever hypertention ( systolic pressure>180mmHg, diastolic pressure>110mmHg), esophageal reflux disease, having sedative, antiemetic or anti-Itch drugs 24 hours before operation, pregnancy or lactation,and those unable to comprehend verbal instruction were removed from this clinical trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| PCIA times in wards;analgesic does consumption;length of first first patient control intravenous analgesia since returning to wards ;extubation time;NRS scores;Analgesic satisfaction;Pain type; | — |
Secondary
| Measure | Time frame |
|---|---|
| FAS scores;rescues analgesia rate in PACU;First exhaust time;First feeding time;First activity time; | — |
Countries
China
Contacts
Public ContactLichun Han
Shaanxi province tumor hospital
Outcome results
None listed