Skip to main content
OpenTrials
Completed

NCT Number: NCT04475029

Methadone in Cystectomy Patients

The role of a single-dose intraoperative methadone on postoperative pain and opioid consumption in patients undergoing Surgeon Accuracy Robot Assistant cystectomy. A prospective double-blind, randomized controlled trial investigating the effect of a single-dose of intraoperative methadone in patients undergoing robotassisted cystectomy.

Completed

Looking for future studies?

Notify Me

Key information

About this study

During early recovery after surgery, intravenous opioids are typically administered to control the pain, either as intermittent bolus administration by nursing staff or by a patient-controlled analgesia device. Unfortunately, repeated doses or boluses of shorter-acting opioids, such as morphine, oxycodone and fentanyl, result in fluctuating blood concentrations, with the inherent risk of only relatively brief periods of adequate pain relief. Moreover, the use of shorter-acting opioids increases the risk of opioid-associated side effects, such as sedation, nausea and vomiting. An alternative approach to the postoperative use of shorter-acting opioids is therefore called for.

In this respect, methadone is an opioid with unique pharmalogical properties that may be advantageous when applied intraoperatively. A single-dose of this long acting opioid could provide a stable analgesia and potentially reduce the need for shorter-acting opioids

Method:

110 patients will be included in an investigator-initiated, prospective, randomised, double-blind, controlled trial with two arms: intervention arm (methadone 0.15 mg/kg ideal body weight). Control arm (morphine 0.15 mg/kg ideal body weight). The study will be GCP-monitored, and is approved by the Danish Health and Medicines Authority (2020041652) and the Central Denmark Region Committees on Health Research Ethics (1-10-72-275-19).

Hypothesis We hypothesize that a single-dose of intravenous intraoperative methadone is efficient and safe for the treatment of postoperative pain after cystectomy.

Objectives The primary objective is to determine whether a single-dose of intravenous methadone reduces postoperative opioid consumption when compared to morphine. The secondary objectives are to compare the effect and safety of intravenous methadone and morphine on postoperative pain, side effects, patient satisfaction and length of stay.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • All patients (≥18 years) scheduled for elective robot assisted cystectomy.

Exclusion criteria

  • American Society of Anesthesiologists (ASA) physical status IV or V
  • Prolonged QTc-interval assessed by electrocardiogram (> 440 milliseconds)
  • Existing treatment with a high risk of QTc-interval prolongation
  • Allergy to study drugs
  • Preoperative daily use of opioids
  • Inability to provide informed consent
  • Severe respiratory insufficiency (oxygen treatment at home)
  • Heart failure (ejection fraction < 30%)
  • Acute abdominal pain
  • Signs of severe liver dysfunction (cirrhosis, inflammation/hepatitis or liver malignancy)
  • Severe kidney insufficiency (estimated Glomerular Filtration Rate < 30 ml/min)
  • Treatment with rifampicin
  • Phaeochromocytoma
  • Treatment with MAO-inhibitor during the last 14 days
  • Pregnancy
  • Nursing mothers
  • Intraoperative conversion to open surgery (secondary inclusion criterion)
  • Epidural analgesia in relation to surgical procedure

Treatment and study plan

Methadone

Drug

One intravenous administration of methadone (0.15 mg/kg treatment weight (height(cm)-100)) one hour prior to expected extubation.

Morphine

Drug

One intravenous administration of morphine (0.15 mg/kg treatment weight (height(cm)-100)) one hour prior to expected extubation.

Primary outcomes

  1. Opioid consumption (morphine mg equivalents)

    Time frame: 3 hours

    • Opioid consumption within the first 3 hours after extubation
  2. Opioid consumption (morphine mg equivalents)

    Time frame: 24 hours

    • Opioid consumption within the first 24 hours after extubation

Secondary outcomes

  1. Pain intensity

    Time frame: within 24 hours

    NRS (0-10) at rest and when coughing. Questionnaires answered by nurse.

  2. Opioid consumption (morphine mg equivalents)

    Time frame: 72 hours

    • Opioid consumption within the first 72 hours after extubation
  3. PONV

    Time frame: Within 24 hours

    • Nausea and/or vomiting (PONV) on a 4-point Likert scale (none/mild/moderate/severe). Questionnaires answered by nurse.
  4. Level of sedation

    Time frame: 3 hours

    Level of sedation (Ramsey Sedation Score) assessed by PACU nurse.

  5. Adverse events

    Time frame: 6 hours

    Any adverse events registered.

  6. Patient satisfaction from 0-10.

    Time frame: 24 hours

    Patient satisfaction with pain management (NRS 0-10) Questionnaires answered by nurse.

  7. Discharge

    Time frame: 6 days

    • Time from arrival to discharge from PACU and hospital (hours and minutes)

Other outcomes

  1. Pain intensity

    Time frame: 32-72 hours

    • Pain intensity (NRS, 0-10) at rest and coughing, questionnaires answered by nurse.
  2. PONV

    Time frame: 32-72 hours

    • Nausea and/or vomiting (PONV) on a 4-point Likert scale (none/mild/moderate/severe). Questionnaires answered by nurse.
  3. Gastrointestinal function

    Time frame: 6-72 hours

    Gastrointestinal function (flatus, stools) and laxatives ordained.

Sponsors and collaborators

Lead sponsor

University of Aarhus

Other

Registry information

Official study title

Clinical Effectiveness and Safety of Intraoperative Methadone in Patients

Acronym: METAMORF

Important dates

Study start
2020
Primary completion
2023
Study completion
2023
First posted
Jul 17, 2020
Registry last updated
Sep 13, 2023

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.

Published trials that share one or more normalized conditions with this study.