The relationship between intervention in administration time of intraoperative analgesics and postoperative pain in wisdom teeth extraction under general anesthesia.
- Conditions
- pericoronitis
- Registration Number
- JPRN-UMIN000045554
- Lead Sponsor
- Showa University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 26
Not provided
1)Patients with contraindications to acetaminophen Patients with aspirin asthma. Patients with severe liver disorder, renal disorder cardiac dysfunction, blood abnormality. Patients with peptic ulcer. Patients with a history of hypersensitivity to acetaminophen. 2)Patients using supplementary analgesics. 3)atients who are contraindicated for the administration of dental 2% lidocaine. Patients with hypertension, arteriosclerosis, heart failure, hyperthyroidism, diabetes mellitus and history of vascular spasm. 4)Patients with a history of hypersensitivity to general anesthetic. 5)Patients with painful oral complications that may affect the efficacy evaluation. 6)Patients scheduled for surgery other than tooth extraction. 7)Patients who cannot communicate and cannot express pain. Patients who have difficulty operating peripheral nerve stimulators. 8)Patients who had other wisdom teeth extracted before 45 days. 9)Patients who have used other non-steroidal anti-inflammatory drugs or antipyretic analgesics including topical drugs before 2 days. 10)Patients with BMI 30 or above. 11)Patients who are pregnant or breast-feeding.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Degree and presence of postoperative pain.
- Secondary Outcome Measures
Name Time Method consciousness level, vital signs, adverse event