KCT0009639
Recruiting
未知
Compare the Safety, Efficacy, and Opioid Consumption of Maxigesic and Paracetamol for Pain Control in the Recovery Room Following Maxillofacial Surgery
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Symptoms, signs and abnormal clinical and laboratory findings, NEC
- Sponsor
- Seoul National University Dental Hospital
- Enrollment
- 72
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •? Patients aged 19 to 60 years old
- •? Patients who are American Society of Anesthesiologists physical status I or II
- •? Patients who are scheduled for double jaw surgery
- •? Patients with body mass index (BMI) between 18\.5 and 30 kg/m2
Exclusion Criteria
- •? Patients with hypersensitivity or allergy to NSAIDs, opioids, acetaminophen
- •? Patients taking medications that may affect clinical trial results, such as pain relievers, sedatives, and psychiatric medications
- •? Patients who are pregnant or breastfeeding
- •? Patients with liver, kidney or brain dysfunction
- •? Contraindications to NSAIDs or paracetamol, such as previous gastric ulcer, heart failure, renal failure, thrombocytopenia, liver dysfunction, asthma, nasal polyps, hypersensitivity to the drug, and patients taking heavy alcohol.
- •? Patients for whom VAS evaluation is expected to be impossible
- •? Patient with pain before surgery
- •? Patients weighing less than 50 kg
- •? Other patients determined by the investigator to be excluded
Outcomes
Primary Outcomes
Not specified
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