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NCT Number: NCT02942550

Methylnaltrexone as a Method to Improve Ticagrelor Uptake in Morphine Treated STEMI Patients

This study will examine the impact of the peripheral opioid antagonist methylnaltrexone on the onset of effect of ticagrelor in morphine treated patients with ST elevation myocardial infarction (STEMI). Half of the participants will receive methylnaltrexone, while the other half will receive placebo.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Karolinska University Hospital, Stockholm, Sweden

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About this study

The rate of drug absorption in the gastro-intestinal tract is often determined by the rate of gastric emptying. Morphine treatment, which is frequently given in order to relieve pain in patients with STEMI, is known to delay gastric emptying, and has indeed emerged as a predictor of delayed/poor antiplatelet response in patients receiving oral prasugrel or ticagrelor.

In recent years, morphine has been found to delay the onset of oral P2Y12-inhibitors. To counteract this, the investigators hypothesized that an opioid antagonist may be used. The opioid antagonist naloxone has previously been shown to reduce the morphine induced delay in gastric emptying However, naloxone crosses the blood-brain barrier (BBB) and reduces the pain relieving effects of morphine. In contrast, the morphine antagonist methylnaltrexone has a reduced passage over the BBB and acts primarily as a peripheral morphine antagonist without affecting the morphine-mediated central analgesic effects.

The aim of the planned study is to evaluate whether methylnaltrexone bromide may reduce the morphine induced delay in onset of platelet inhibition after a loading dose of 180 mg ticagrelor in morphine treated patients with STEMI undergoing primary percutaneous coronary intervention (PCI), where a rapid and adequate platelet inhibition after the administration of ticagrelor is crucial. As morphine is an inclusion criterion, all patients included in the study will be on morphine treatment. Thus, morphine treatment is not an intervention to be administered as part of the protocol. Stratification according to inferior and anterior/lateral STEMI will be perform to avoid imbalance in the location of myocardial infarction between the groups.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Diagnosis of STEMI
  • Administration of a 180 mg loading dose ticagrelor
  • Analgesic treatment with intravenous morphine pre-PCI

Exclusion criteria

  • Cardiac arrest
  • Body weight > 114kg
  • Vomiting after intake of ticagrelor loading dose
  • Use of Naloxone before inclusion or during sampling period
  • Inability to understand study outline and instructions
  • Methylnaltrexone bromide contraindication
  • Age <18 years; 8) Women in fertile age
  • Administration of ticagrelor during the week before inclusion
  • Treatment with Cangrexal
  • Ongoing long-term opioid treatment.

Treatment and study plan

Methylnaltrexone bromide (Relistor®).

Drug

Sodium Chloride 9mg/mL

Drug

Primary outcomes

  1. High on-treatment platelet reactivity (HPR)

    Time frame: Two hours after the injection of either active drug or placebo

    HPR defined as platelet reactivity index (PRI) ≥50% using VASP analysis

  2. Number of participants with serious adverse events

    Time frame: Within 48 hours after drug administration

    Serious AE is any untoward medical occurrence that at any dose:

    • Results in death.
    • Is life-threatening at the time of the event.
    • Requires inpatient hospitalization.
    • Requires prolongation of existing hospitalization.
    • Results in persistent or significant disability/incapacity.
    • Is a congenital anomaly/birth defect.

Secondary outcomes

  1. High on-treatment platelet reactivity

    Time frame: One hour after the injection of either active drug or placebo

  2. Difference in ticagrelor and AR-C124910XX concentrations

    Time frame: One and two hours after the injection of either active drug or placebo

  3. Change in patient pain according to visual analog scale

    Time frame: One and two hours after the injection of either active drug or placebo

  4. Difference in ticagrelor and AR-C124910XX concentrations between patients with inferior STEMI and patients with anterior/lateral STEMI.

    Time frame: One and two hours after the injection of either active drug or placebo

  5. Difference in high on-treatment platelet reactivity (HPR) between patients with inferior STEMI and patients with anterior/lateral STEMI.

    Time frame: One and two hours after the injection of either active drug or placebo

    HPR defined as platelet reactivity index (PRI) ≥50% using VASP analysis

Sponsors and collaborators

Lead sponsor

Karolinska University Hospital

Other

Registry information

Official study title

Methylnaltrexone as a Method to imprOVE Platelet Inhibition of Ticagrelor in Morphine-treated Patients With ST-segMENT Elevation Myocardial Infarction: a Prospective, Single Blinded Randomized, Placebo-controlled Trial

Acronym: MOVEMENT

Important dates

Study start
2016
Primary completion
2017
Study completion
2017
First posted
Oct 24, 2016
Registry last updated
Apr 9, 2018

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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