Overview

Intravenous Acetaminophen/Ibuprofen Fixed-dose Combination on Postoperative Opioid Consumption

Status:
Not yet recruiting
Trial end date:
2024-05-30
Target enrollment:
0
Participant gender:
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/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Seoul National University Hospital
Collaborator:
Kyongbo Pharmaceutical
Treatments:
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