Evaluating pain relief with Maxigesic in breast cancer surgery

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study investigates the effectiveness and safety of Maxigesic, a combination of acetaminophen and ibuprofen, as a perioperative analgesic for patients undergoing breast cancer surgery. The goal is to provide adequate pain relief while minimizing immune compromise associated with opioid use. Participants will receive Maxigesic in conjunction with opioid-based intravenous patient-controlled analgesia (IV-PCA) during their surgical procedure. The study focuses on patients aged 20 to 70 with specific health classifications undergoing cancer resection or reconstruction.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Patient aged 20 to 70 years with ASA classification 1 to 3 undergoing breast cancer surgery (cancer resection or reconstruction)

Exclusion Criteria:

* ASA classification 4/ allergy to acetaminophen, NSAIDs, opioid/ severe liver or renal dysfunction/ pregnancy

Where it's running

• Department of Anesthesiology and Pain Medicine, Yonsei University College of Medicine
  Seoul, South Korea Recruiting

Study contacts

• Study coordinator: Jin Sun Cho
• Email: chjs0214@yuhs.ac
• Phone: 82-2-2228-2419

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.