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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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 4
Primary location
Karolinska University Hospital, Stockholm, Sweden
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
Sodium Chloride 9mg/mL
DrugPrimary outcomes
-
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
-
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
-
High on-treatment platelet reactivity
Time frame: One hour after the injection of either active drug or placebo
-
Difference in ticagrelor and AR-C124910XX concentrations
Time frame: One and two hours after the injection of either active drug or placebo
-
Change in patient pain according to visual analog scale
Time frame: One and two hours after the injection of either active drug or placebo
-
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
-
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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