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Clinical Trials/KCT0009290
KCT0009290
Not yet recruiting
未知

Comparison of the opioid-sparing effect of preemptive and preventive intravenous acetaminophen/ibuprofen fixed-dose combination after hand-assisted laparoscopic nephrectomy: A randomized controlled trial

Ajou University Hospital0 sites42 target enrollmentTBD
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Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Ajou University Hospital
Enrollment
42
Status
Not yet recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

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

Investigators

Sponsor
Ajou University Hospital

Eligibility Criteria

Inclusion Criteria

  • •A. Patients aged 19 to 80 years undergoing hand\-assisted laparoscopic nephrectomy
  • •B. Patients who can provide written consent to participate in the clinical study, understand the procedures of this clinical study, and appropriately complete the patient\-reported questionnaire.
  • •C. American Society of Anesthesiologists physical status classification (ASA physical status classification) grade 1\-2

Exclusion Criteria

  • •A. Patients who did not consent to the study
  • •B. American Society of Anesthesiologists physical status classification (ASA physical status classification) grade 3\-4
  • •C. Patients who are chronically taking opioids
  • •D. Patients who have other severe pain at the time of screening, which may cause confusion in pain evaluation
  • •E. Patients with hypersensitivity to acetaminophen, ibuprofen, fentanyl, or local anesthetics
  • •F. Patients with a history of gastric ulcer or gastrointestinal bleeding
  • •G. Patients with liver failure, renal failure, or heart failure
  • •H. Patients with alcoholism
  • •I. Patients taking anticoagulant drugs or having blood coagulation abnormalities
  • •J. Patients with bronchial asthma

Outcomes

Primary Outcomes

Not specified

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