Key result
This is a study protocol describing a planned randomized trial to evaluate the influence of metoclopramide on the pharmacokinetics and pharmacodynamics of ticagrelor; no results are available yet.
Why the study?
Does metoclopramide improve the pharmacokinetic and pharmacodynamic profile of ticagrelor in patients with unstable angina pectoris receiving concomitant treatment with morphine?
Does metoclopramide improve the pharmacokinetic and pharmacodynamic profile of ticagrelor in patients with unstable angina pectoris receiving concomitant treatment with morphine?
This study protocol outlines a randomized trial to determine if metoclopramide can overcome the delayed absorption and antiplatelet effect of ticagrelor caused by concomitant morphine administration in patients with unstable angina.
Answers are grounded in this paper and cite their sources.
Metoclopramide's role in countering morphine-ticagrelor interaction remains unproven; RCT will deliver first randomized data in unstable angina.
Introduction. Nowadays, due to the “morphine effect”, the screening of methods that provide quick and effective platelet inhibition with oral P2Y12 inhibitors administrated simultaneously with morphine in patients with acute coronary syndromes are extensively investigated by numerous scientists. Metoclopramide, which stimulates the motility of gastrointestinal tract, may become a potential method of overcoming the negative morphine effect. The present study was designed to demonstrate the influence of metoclopramide administration on the pharmacokinetic and pharmacodynamic profile of ticagrelor between patients with unstable angina pectoris treated with morphine and crushed ticagrelor. Methods/design. A study was designed as a phase IV, single-centre, randomized, investigator-initiated, parallel-group, open-label, interventional trial. Patients will be randomized in a 1:1 manner into two arms: 1) patients treated with a combination of crushed ticagrelor and morphine and 2) patients treated with a combination of crushed ticagrelor followed by morphine and metoclopramide. Blood sample collection will be scheduled directly before the administration of ticagrelor loading dose and 15, 30, 45, 60, 120, 180, 240, and 360 minutes after the loading dose. Pharmacokinetic and pharmacodynamic assessment of ticagrelor and its active metabolite will be evaluated in all pre-defined time points. Discussion. The current study is, to our knowledge, the first one to provide data on the influence of metoclopramide in patients with acute coronary syndromes, who received intravenous opioid analgesia. It is expected to contribute to the development of contemporary knowledge on the treatment of patients presenting with acute coronary syndromes, and should enable clinicians to implement strategies of quick platelet inhibition.
No takes yet. Share an insight, caveat, or question.
Sikora et al. (2016) studied Unstable angina pectoris. Metoclopramide vs. Crushed ticagrelor and morphine without metoclopramide was evaluated on Time to maximum concentration (tmax) for ticagrelor and AR-C124900XX within 6 hours. This is a study protocol describing a planned randomized trial to evaluate the influence of metoclopramide on the pharmacokinetics and pharmacodynamics of ticagrelor; no results are available yet.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: