KCT0003896Recruiting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
Trial Snapshot
- Phase
- 未知
- Status
- Recruiting
- Sponsor
- Asan Medical Center
- Enrollment
- 246
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional Study
Eligibility Criteria
- Ages
- 20(Year) to 70(Year) (—)
- Sex
- All
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.
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