Status:
COMPLETED
Intravenous Acetaminophen/Ibuprofen Fixed-dose Combination on Postoperative Opioid Consumption
Lead Sponsor:
Seoul National University Hospital
Collaborating Sponsors:
Kyongbo Pharmaceutical
Conditions:
Postoperative Pain
Eligibility:
All Genders
19-80 years
Phase:
NA
Brief Summary
This prospective, randomized, double-blinded study is designed to evaluate the postoperative analgesic effect of the intravenous acetaminophen/ibuprofen fixed-dose combination in patients undergoing v...
Detailed Description
Adult patients undergoing elective unilateral VATS wedge resection, segmentectomy, or lobectomy are randomly allocated to receive intravenous acetaminophen (1000 mg)/ibuprofen (300 mg) fixed-dose comb...
Eligibility Criteria
Inclusion
- Patients scheduled to undergo elective unilateral VATS segmentectomy or lobectomy under general anesthesia
- American Society of Anesthesiologists (ASA)physical classification I-II
- Consent to IV-patient controlled analgesia use
- Willingness and ability to sign an informed consent document
Exclusion
- Do not understand our study
- Allergies to anesthetic or analgesic medications
- Continuous local anesthetics infiltration for postoperative pain control
- Patients who receive mechanical ventilation more than 2 hours after surgery
- Pregnancy/Breastfeeder
- Medical or psychological disease that can affect thetreatment response
Key Trial Info
Start Date :
October 3 2022
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 15 2023
Estimated Enrollment :
96 Patients enrolled
Trial Details
Trial ID
NCT05366777
Start Date
October 3 2022
End Date
October 15 2023
Last Update
December 19 2023
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Seoul National University Hospital
Seoul, South Korea, KS013