A comparison of intravenous nefopam and fentanyl for patient controlled analgesia in patients with two jaw surgery
Not Applicable
Recruiting
- Conditions
- Not Applicable
- Registration Number
- KCT0001592
- Lead Sponsor
- Seoul National University Dental Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 174
Inclusion Criteria
Patients who agree with the study receive the intravenous patient controlled analgesia after two jaw surgery. They are belonged to American Society of Anesthesiologists classification I,II or III, aged 20 to 40.
Exclusion Criteria
Patients aged under 20 years old, patients under the emergency operations, patients who had already the sedatives or analgesic drug which could have impact on the sleep or pain. Patients with the chronic obstructive pulmonary disease or asthma. Patients who had the upper respiratory infection within 2 weeks. Patient who have chronic pain disease, smoker, heart disease, hepatic disease or kidney disease. In addition patients who are identified to be inappropriate for the study by physician.
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method the postoperative nausea and vomiting(PONV)
- Secondary Outcome Measures
Name Time Method the postoperative pain;The postoperative shivering;The quality of sleep;The satisfaction from the PCA;The total volume of infusion, times of bolus attempt, times of bolus infusion;The dose of additive analgesics and additive antiemetics