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NCT Number: NCT07226245

Methadone Pharmacokinetics in Cardiac Surgery

Cardiac surgery frequently leads to significant postoperative pain, with multiple different drug regimens being utilized (both opioid and non-opioid) in an attempt to alleviate this surgical pain. Methadone is currently one of the drugs that is being utilized to help control the pain. It can be given during and/or after surgery. This study hopes to identify the optimal dose of methadone to use to treat this surgical pain.

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Wake Forest University Health Sciences

Winston-Salem, North Carolina, 27157, United States

Location contact

Ettore Crimi, MD

PRINCIPAL_INVESTIGATOR

Lynnette Harris, BSN, RN

CONTACT

[email protected]

336-306-0778

About this study

The uncertainty regarding optimal methadone dosing and the necessity of post-cardiopulmonary bypass (CPB) supplementation provides a compelling rationale for this study. Specifically, it remains unknown whether a single higher initial dose of methadone can adequately maintain analgesic plasma concentrations throughout cardiac surgery and recovery, or if a split-dosing strategy administering a lower initial dose followed by an additional dose post-CPB might offer similar or improved analgesic outcomes with fewer side effects. This study will evaluate pharmacokinetics of methadone using three different dosing strategies in patients undergoing cardiac surgery with CPB.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Elective cardiac surgery requiring median sternotomy and cardiopulmonary bypass (CABG, valve, combined CABG/valve surgeries)
  • Anticipated extubation within 12 hours postoperatively
  • No prior opioid use within 30 days of surgery
  • Ability to provide informed consent

Exclusion criteria

  • Severe liver or kidney dysfunction (Child-Pugh class B/C, eGFR <30 mL/min/1.73m², creatinine >2 mg/dL, dialysis)
  • Allergy to methadone or fentanyl
  • Use of CYP3A4 inducers (rifampin, phenytoin, carbamazepine), CYP3A4 inhibitors (ketoconazole, erythromycin, clarithromycin, itraconazole), SSRIs (fluoxetine, sertraline, paroxetine, citalopram, escitalopram, fluvoxamine)
  • Body mass index >40 kg/m²
  • Corrected QT interval interval >500 milliseconds
  • Intubation anticipated >12 hours
  • History of illicit drug use or alcohol or opioid abuse use disorder within last 12 months
  • Mechanical circulatory support, heart transplant, deep hypothermic circulatory arrest procedures
  • Left Ventricular Ejection Fraction <30%
  • Pulmonary disease requiring oxygen therapy
  • Preoperative inotropic support or intra-aortic balloon pump
  • Emergency surgery
  • Postoperative regional anesthesia
  • Hemofiltration during cardiopulmonary bypass

Treatment and study plan

Single dose of methadone

Drug

Single dose of methadone 0.3 mg/kg actual body weight (max 30 mg) administered at induction of anesthesia

Split dose of methadone

Drug

Split dose of methadone 0.2 mg/kg actual body weight at induction and 0.1 mg/kg actual body weight post cardiopulmonary bypass

Balanced split dose of methadone

Drug

Balanced split dose of methadone 0.15 mg/kg actual body weight at induction and 0.15 mg/kg actual body weight post cardiopulmonary bypass

Primary outcomes

  1. Plasma methadone concentration (ng/mL) 10 min post initial dose

    Time frame: 10 minutes

    Plasma methadone concentration will be measured 10 minutes post initial methadone dose

  2. Plasma methadone concentration (ng/mL) 30 min post initial dose

    Time frame: 30 minutes

    Plasma methadone concentration will be measured 30 minutes post initial methadone dose pre cardiopulmonary bypass

  3. Plasma methadone concentration (ng/mL) 60 min post initial dose

    Time frame: 60 minutes

    Plasma methadone concentration will be measured 60 minutes post initial methadone dose pre cardiopulmonary bypass

  4. Plasma methadone concentration (ng/mL) 10 min post start of cardiopulmonary bypass

    Time frame: 10 minutes

    Plasma methadone concentration will be measured 10 minutes after cardiopulmonary bypass started

  5. Plasma methadone concentration (ng/mL) 30 min post start of cardiopulmonary bypass

    Time frame: 30 minutes

    Plasma methadone concentration will be measured 30 minutes after cardiopulmonary bypass started

  6. Plasma methadone concentration (ng/mL) 60 min post start of cardiopulmonary bypass

    Time frame: 60 minutes

    Plasma methadone concentration will be measured 60 minutes after cardiopulmonary bypass started

  7. Plasma methadone concentration (ng/mL) 10 min post cardiopulmonary bypass completion

    Time frame: 10 minutes

    Plasma methadone concentration will be measured 10 minutes after cardiopulmonary bypass ended

  8. Plasma methadone concentration (ng/mL) 120 min post start of cardiopulmonary bypass

    Time frame: 120 minutes

    Plasma methadone concentration will be measured 120 minutes after cardiopulmonary bypass started

  9. Plasma methadone concentration (ng/mL) before first analgesic request

    Time frame: up to 72 hours

    Plasma methadone concentration will be measured at the time of first analgesic request by participant

  10. Plasma methadone concentration (ng/mL) 3 hours post Intensive Care Unit arrival

    Time frame: 3 hours

    Plasma methadone concentration will be measured 3 hours post Intensive Care Unit arrival

  11. Plasma methadone concentration (ng/mL) 12 hours post Intensive Care Unit arrival

    Time frame: 12 hours

    Plasma methadone concentration will be measured 12 hours post Intensive Care Unit arrival

  12. Plasma methadone concentration (ng/mL) 24 hours post Intensive Care Unit arrival

    Time frame: 24 hours

    Plasma methadone concentration will be measured 24 hours post Intensive Care Unit arrival

Secondary outcomes

  1. pain intensity score

    Time frame: 2, 4, 8, 12, 24, 48, and 72 hours postoperatively and month 3

    Pain intensity score will be measured using the visual analog scale. Scores will be measured on a scale of 0-10, with 0=no pain and 10=most severe pain

  2. patient global impression of change

    Time frame: 24, 48, and 72 hours after removal of the breathing tube

    Patient Global Impression of Change will be used to assess patient-perceived analgesic effectiveness and overall postoperative recovery. Total score range is 1-7 with a higher score indicating considerable improvement with treatment.

  3. postoperative opioid consumption

    Time frame: up 72 hours postop

    total postoperative opioid consumption in morphine milligram equivalents

  4. duration of postoperative mechanical ventilation

    Time frame: up to 72 hours postop

    number of minutes with postoperative mechanical ventilation

  5. time of ambulation

    Time frame: up to 48 hours postop

    number of minutes until patient first ambulates after surgery

  6. length of Intensive Care Unit stay

    Time frame: up to 3 days postop

    number of hours spent in Intensive Care Unit

  7. length of hospital length stay

    Time frame: up to 7 days postop

    number of days spent in hospital

Study contacts

Contact information is provided by the study sponsor or research team.

Ettore Crimi, MD

CONTACT

[email protected]

336-716-4498

Lynnette Harris, BSN

CONTACT

[email protected]

336-716-8791

Sponsors and collaborators

Lead sponsor

Wake Forest University Health Sciences

Other

Registry information

Official study title

Evaluating Pharmacokinetics of Three Methadone Dosing Strategies During Cardiac Surgery With Cardiopulmonary Bypass

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Nov 10, 2025
Registry last updated
May 26, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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