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.
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.
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
- Conditions
- Patients Treated With Methadone
- 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 group | Role | What they receive |
|---|---|---|
| ICU patients treated with methadone | Not 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.
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.
- First posted23 Oct 2026
- Study start1 Jan 2027 (estimated)
- Primary completion1 Jan 2028 (estimated)
- Study completion1 Jan 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Patients Treated With MethadoneStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Meir Medical Center
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, sara dichtwald, Meir Medical Center
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
Study at a glance
From the registry record, last updated by the sponsor on 23 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Methadone Administration in Critically Ill Patients in the Intensive Care Unit and Risk of Prolonged QTc and Cardiac Arrythmia: a Retrospective Study
- ClinicalTrials.gov ID
- NCT07892677
- Acronym / sponsor ID
- MMC-0412-26
- Conditions
- Patients Treated With Methadone
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 300 participants (estimated)
- Lead sponsor
- Meir Medical CenterUniversity, hospital or other
- Study start
- 1 Jan 2027 (estimated)
- Primary completion
- 1 Jan 2028 (estimated)
- Study completion
- 1 Jan 2028 (estimated)
- First posted
- 23 Oct 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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
Study design
- Observational model
- Cohort
- Time perspective
- Retrospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| ICU patients treated with methadone | – | Drug: ICU patients treated with methadone |
Who may qualify
- Ages
- 18 to 99 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- ICU patients who were treated with methadone during ICU stay
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| ICU patients treated with methadoneICU patients treated with methadone | Drug | ICU patients treated with methadone |
Primary outcome
QTc prolongation
Time frame: Through study completion, an average of 1 year
Fatal ventricular arrythmia
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 23 Oct 2026.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
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.