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Clinical Trials/KCT0003896
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

Asan Medical Center0 sites246 target enrollmentTBD

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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional Study
Sex
All

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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