AzTrials
AzTrials

Patients Treated With MethadoneNCT07892677

Methadone Administration in Critically Ill Patients in the Intensive Care Unit and Risk of Prolonged QTc and Cardiac Arrythmia

An observational study of Patients Treated With Methadone, run by Meir Medical Center at 1 site in Israel.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
Search all trials

Trial summary

Continuous infusion of short-acting synthetic opioids, primarily remifentanil, is widely used for anesthesia and analgesia in ventilated patients in the intensive care unit (ICU) due to its short half-life, which is independent of hepatic or renal clearance, which may be reduced or unpredictable in these patients… Read more about this study

Who is it for?
Ages 18 to 99 years
Conditions the study is for
Patients Treated With Methadone
What is being tested?
ICU patients treated with methadone
How many people
300 participants
Where
1 siteIsrael
Study dates
1 Jan 2027to 1 Jan 2028
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 99 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: ICU patients who were treated with methadone during ICU stay

Inclusion Criteria: ICU patients from 1.2022 to 10.2026 who were treated with methadone during ICU stay -

Exclusion Criteria: Patients who recieved methadone prior to ICU admission, or when data regarding QTc interval or arrythmia are missing

-

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Israel1 site
  • Meir Medical Center

    Kfar Saba

Other trials in Israel

About this study

Official title: Methadone Administration in Critically Ill Patients in the Intensive Care Unit and Risk of Prolonged QTc and Cardiac Arrythmia: a Retrospective Study

Continuous infusion of short-acting synthetic opioids, primarily remifentanil, is widely used for anesthesia and analgesia in ventilated patients in the intensive care unit (ICU) due to its short half-life, which is independent of hepatic or renal clearance, which may be reduced or unpredictable in these patients [1,2]. However, prolonged exposure results in rapid development of drug tolerance, opioid-induced hyperalgesia (OIH), and severe iatrogenic opioid withdrawal syndrome (IOWS) with abrupt discontinuation or rapid down-titration of the drug [1-3]. IOWS is characterized by withdrawal symptoms including delirium, restlessness, increased blood pressure, onset of sharp pain, increased respiratory and heart rates, and consequently increased metabolic demand. All of the above are undesirable and potentially dangerous in critically ill patients, and may compromise the chances of successful respiratory withdrawal in these patients [2,4].

To alleviate these symptoms and facilitate successful respiratory withdrawal, a long-acting opioid, such as methadone, can be used as a bridge. The use of a long-acting opioid may help prevent opioid withdrawal syndrome. Clinical protocols exist for the use of enteral methadone (oral or via gavage) for this purpose [2,4,5]. Methadone is a fully synthetic μ-opioid receptor agonist with high gastrointestinal bioavailability (>80%) and a long half-life (15-60 hours) [2,6]. This pharmacokinetic profile provides sustained plasma concentrations that avoid the sharp troughs associated with infusion of a short-acting opiate [5,6]. Furthermore, methadone acts as a non-competitive antagonist at the N-methyl-D-aspartate (NMDA) receptor [6,7]. By reducing central NMDA-mediated sensitization, methadone reduces OIH and attenuates acute tolerance that develops during chronic exposure to remifentanil, making it an effective pharmacological "bridger" in intensive care [2,5,7]. Methadone's activity at the NMDA receptor also has an analgesic effect that is not mediated through opioid receptors. Methadone is not cleared renally, so renal failure, which is common in critically ill patients, does not affect its clearance. Even in situations of hepatic insufficiency, very severe liver damage is required to have an effect on methadone clearance, an additional advantage of its use in critically ill patients. In addition, compared to other opioids (such as OxyContin or Fentanyl), methadone does not produce a significant euphoric feeling, which reduces its potential for addiction.

Read more

Although methadone is an old and well-known substance, and despite its advantages as discussed above, along with the existence of treatment protocols [4,5], the use of methadone in the intensive care unit remains limited due to concerns about the potential for the development of fatal cardiac arrhythmias with its use [1,8]. Methadone inhibits the delayed rectifier potassium current (I_Kr) by blocking the anthraquinone-related gene (hERG) potassium channel, which may delay ventricular repolarization, prolong the corrected QT interval (QTc), and predispose patients to dangerous arrhythmias such as torsades de pointes (TdP [1,8,9]. Furthermore, many patients in intensive care receive other medications that may prolong the QTc interval (macrolide or fluoroquinolone antibiotics, antipsychotics for the treatment of delirium such as haloperidol or Zyprexa, gastrointestinal motility agents such as peramin or erythromycin, etc.) and/or have other disorders that may prolong the QTc interval, such as hypokalemia, hypomagnesemia, or hypocalcemia.

However, current perceptions regarding Methadone-induced arrhythmias are largely derived from patients receiving methadone maintenance therapy (MMT) in outpatient settings for the treatment of chronic opioid use disorder [1,3,8]. These outpatient treatment groups differ substantially from critically ill patients in intensive care undergoing short-term opiate withdrawal protocols [1,8,9]. MMT regimens routinely use high, sometimes escalating doses of methadone (often >100-120 mg/day) over years, these patients often take other unregulated illicit substances in addition to their "legal" methadone treatment (opioid drugs, drugs from other classes, or prescription drugs taken illegally), and these patients often have other metabolic disorders resulting from their general poor condition (malnutrition, dehydration, untreated electrolyte abnormalities, and other chronic diseases). [1,8,9]. In contrast, protocols for administering methadone to patients in intensive care include significantly lower doses of the drug administered for a relatively short period of time (days to weeks, in exceptional cases months, typical doses of 20-60 mg per day for most patients), patients are under continuous cardiac monitoring (ECG monitor, in some cases, as in our unit, there is also continuous monitoring of the QTc interval throughout the day), monitoring of potassium, magnesium and calcium values and clinical pharm

Being tested
ICU patients treated with methadone

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • ICU patients treated with methadoneDrug

    ICU patients treated with methadone

Study groups in NCT07892677
Study groupRoleWhat they receive
ICU patients treated with methadoneNot described
Receives: Drug: ICU patients treated with methadone

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. QTc prolongation

    Fatal ventricular arrythmia

    Measured: Through study completion, an average of 1 year

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted23 Oct 2026
  2. Study start1 Jan 2027 (estimated)
  3. Primary completion1 Jan 2028 (estimated)
  4. Study completion1 Jan 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Retrospective
Enrolment
300 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07892677
Sponsor's protocol ID
MMC-0412-26
Status last verified
Oct 2026
First submitted
13 Oct 2026
Last updated
23 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of Patients Treated With Methadone, run by Meir Medical Center at 1 site in Israel.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 23 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Israel. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Sara Dichtwald, Dr (972-9-7472133, sara.dichtwald@clalit.org.il), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

QTc prolongation (time frame: Through study completion, an average of 1 year). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Oct 2026.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in