KCT0003896
Recruiting
未知
A Clinical Trial to Evaluate the Analgesic Efficacy and Safety of Nefopam(Acupan®) Compared to Oxycodone (Oxynorm®) in Postoperative Intravenous Patient-Controlled Analgesia of Patients Undergoing General Surgery
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Asan Medical Center
- Enrollment
- 246
- Status
- Recruiting
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients undergoing general anesthesia under laparoscopic gastrointestinal or colorectal surgery
- •\- Patients who applied for postoperative intravenous patient\-controlled analgesia
- •\- American Society of Anesthesiologists Physical Status 1, 2, and 3
Exclusion Criteria
- •\- Patients taking pain medication preoperatively
- •\- Patients who are anaphylactic to nefopam or oxycodone
- •\- Patients with estimated glomerular filtration rate \<60 ml / min / 1\.73 m2
- •\- Patients with a history of epilepsy
- •\- Patients with a history of ischemic heart disease
- •\- Patients taking monoamine oxidase inhibitor
- •\- Patients with walking disorders
- •\- Patients who can not press the analgesic administration button themselves for pain relief when there is postoperative pain due to impaired cognitive function or comprehension.
Outcomes
Primary Outcomes
Not specified
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