Overview
Intravenous Acetaminophen/Ibuprofen Fixed-dose Combination on Postoperative Opioid Consumption
Status:
Not yet recruiting
Not yet recruiting
Trial end date:
2024-05-30
2024-05-30
Target enrollment:
0
0
Participant gender:
All
All
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 video-assisted thoracic surgery (VATS). We hypothesize that the intravenous acetaminophen/ibuprofen fixed-dose combination can significantly reduce postoperative opioid consumption and pain severity in patients with VATS.Phase:
N/AAccepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Seoul National University HospitalCollaborator:
Kyongbo PharmaceuticalTreatments:
Acetaminophen
Ibuprofen
Criteria
Inclusion Criteria:- 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 Criteria:
- 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