The efficacy of the continuous intravenous background infusion regimens optimized by the demand of the patient-controlled analgesia of fentanyl for the acute postoperative pain management
Not Applicable
Completed
- Conditions
- Not Applicable
- Registration Number
- KCT0002156
- Lead Sponsor
- Ajou University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 105
Inclusion Criteria
Patients scheduled for elective gynecological surguries under general anesthesia.
American Society of Anesthesiologists physical status 1,2
Patients who want acute postoperative pain management.
Exclusion Criteria
Body weight over or under 20% of ideal body weight.
Chronic pain
History of drug or alcohol abuse.
Chronic administration of opioids and/or sedatives.
Patients who cannot agree this study voluntarily.
Patients who was taken opioids or analgesics except remifentanil.
Patients who showed delayed recovery of consciousness over 30 minutes after the end of anesthesia.
Patients who need extra treatments due to postoperative complications.
Patients who need postoperative care in the intensive care unit.
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Incidence of inadequate analgesia at PACU (post-anesthesia care unit);incidence of inadequate analgesia when the patient dischages from PACU;visual analogue scale (VAS) pain scores during the first 24 hours after surgery
- Secondary Outcome Measures
Name Time Method Incidences of complications (nausea/vomiting, dizziness, headache, itching);level of consciousness, blood pressure, heart rate;amount of fentanyl administration;Patient controlled analgesia (PCA) supply episode, PCA demand episode, number and time of rescue analgesic administration;overall evaluation of acute pain management (satisfaction), causes of unsatisfaction