# Intravenous methadone for perioperative acute and chronic pain management in Chinese adult cardiac surgical patients: A protocol for pilot randomized controlled trial

**Authors:** Henry Man Kin Wong, Wai Tat Wong, Xiaodong Liu, Sylvia Siu Wah Au, Randolph Hung Leung Wong, Steve Zimmerman, Steve Zimmerman

PMC · DOI: 10.1371/journal.pone.0323820 · PLOS One · 2025-06-02

## TL;DR

This study explores using intravenous methadone for pain management in Chinese cardiac surgery patients to improve recovery and reduce chronic pain.

## Contribution

This is the first pilot trial of intravenous methadone for perioperative pain in Chinese cardiac surgical patients.

## Key findings

- Intravenous methadone may provide long-term pain relief and reduce chronic postsurgical pain.
- Plasma methadone concentration analysis will support future large-scale research on optimized pain management.
- The study will assess feasibility, opioid requirements, and recovery outcomes in cardiac surgical patients.

## Abstract

Postoperative pain is significant in cardiac surgical patients. Perioperative analgesia with intermittent administration of opioids can result in significant fluctuations in serum opioid concentrations. Methadone should provide a rapid onset and long-term pain relief upon a single intravenous dose at induction of anesthesia, and may reduce chronic postsurgical pain (CPSP) in cardiac surgical patients. The feasibility of using intravenous methadone in Chinese cardiac surgical patients, and its effect on acute and chronic pain management after cardiac surgery will be evaluated.

A single-center, prospective, randomized-controlled pilot trial. Adult cardiac surgical patients will be randomized to receive 0.2 mg/kg methadone or morphine at induction of anesthesia. Patient-controlled analgesia morphine protocol, oral paracetamol and dihydrocodeine will be given for postoperative analgesia. Venous blood sampling for plasma methadone concentration will be obtained at regular intervals from study drug infusion to 96 hours after administration. The primary outcome will be a description of study feasibility, encompassing recruitment and retention, protocol adherence and stakeholder acceptability. Secondary outcomes include the time of ventilator weaning to spontaneous breathing, time of extubation, morphine requirements within 24 hours and 72 hours after surgery, time to first morphine rescue, postoperative pain scores, patient satisfaction, and length of stay in ICU and hospital. Opioid-related side effects including sedation, nausea and vomiting, and time to first bowel opening will be recorded. CPSP will be assessed with Neuropathic Pain Scale and Pain Catastrophizing Scale at 3 and 6 months after surgery.

Randomized controlled trials on intravenous methadone in cardiac surgical patients are scarce, with none in Chinese populations. This study, supported by plasma methadone concentration analysis, will establish a basis for future large-scale research aimed at improving recovery through optimized pain management.

ClinicalTrials.gov NCT05913284.

## Linked entities

- **Chemicals:** methadone (PubChem CID 4095), morphine (PubChem CID 5288826), paracetamol (PubChem CID 1983), dihydrocodeine (PubChem CID 3063)

## Full-text entities

- **Diseases:** vomiting (MESH:D014839), Pain (MESH:D010146), nausea (MESH:D009325), acute and chronic pain (MESH:D059787), CPSP (MESH:D010149)
- **Chemicals:** morphine (MESH:D009020), paracetamol (MESH:D000082), Methadone (MESH:D008691), dihydrocodeine (MESH:C014481)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC12129159/full.md

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Source: https://tomesphere.com/paper/PMC12129159