This study is currently not recruiting participants.

Prospective Observational Study of Trauma Patients on Antiplatelet Agents

Study on the Effects of P2Y12 Inhibitors in Trauma Patients

Not Recruiting
100 years or below
All
Phase N/A

Brief description of study.

With the introduction of more potent P2Y12 inhibitors comes a new challenge to trauma surgeons when faced with patients taking these medications. These agents possess more reliable pharmacologic antiplatelet properties than clopidogrel, which is favorable since clopidogrel has been shown to have 25% inhibition of platelet activity in up to 30% of patients. Along with increased platelet inhibition comes increased bleeding events. With promising characteristics of decreased all-cause mortality and cardiovascular events, there has been an increase in these agents use compared to clopidogrel. Little is known about the effect of these agents when a patients is injured. Through examination of various antiplatelet agents, trauma surgeons will gain valuable knowledge when faced with patients taking these medications. Particular areas of information include comparative bleeding events between agents, monitoring for progression of bleeding events, and reversal strategy efficacy and risks. Successful completion of the study?s aims will provide clinical evidence in the management of trauma patients taking antiplatelet agents. As innovation of newer antiplatelet agents occurs, trauma surgeons must gain clinical evidence in the approach to these medications. Through this multicenter, prospective trial, valuable information will assist clinicians in the management of trauma patients taking newer P2Y12 inhibitors. To date, there are no studies examining these newer agents in trauma patients.

Detailed description of study

With the introduction of more potent P2Y12 inhibitors comes a new challenge to trauma surgeons when faced with patients taking these medications. These agents possess more reliable pharmacologic antiplatelet properties than clopidogrel, which is favorable since clopidogrel has been shown to have 25% inhibition of platelet activity in up to 30% of patients. Along with increased platelet inhibition comes increased bleeding events. With promising characteristics of decreased all-cause mortality and cardiovascular events, there has been an increase in these agents use compared to clopidogrel. Little is known about the effect of these agents when a patients is injured. Through examination of various antiplatelet agents, trauma surgeons will gain valuable knowledge when faced with patients taking these medications. Particular areas of information include comparative bleeding events between agents, monitoring for progression of bleeding events, and reversal strategy efficacy and risks. Successful completion of the study?s aims will provide clinical evidence in the management of trauma patients taking antiplatelet agents. As innovation of newer antiplatelet agents occurs, trauma surgeons must gain clinical evidence in the approach to these medications. Through this multicenter, prospective trial, valuable information will assist clinicians in the management of trauma patients taking newer P2Y12 inhibitors. To date, there are no studies examining these newer agents in trauma patients.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: trauma
  • Age: 100 years or below
  • Gender: All

This study investigates the effects of P2Y12 inhibitors on trauma patients. P2Y12 inhibitors are medications that prevent blood cells called platelets from sticking together and forming clots. These medications are stronger than clopidogrel, another drug used for the same purpose, but they may also increase the risk of bleeding.

In this study, researchers will look at different antiplatelet medications to understand how they affect bleeding in trauma patients. They will compare bleeding events, monitor how bleeding progresses, and evaluate the effectiveness and risks of strategies to reverse the effects of these medications.

  • Who can participate: Eligibility criteria are not specified.
  • Study details: Participants in this study will be monitored for bleeding events and may undergo procedures to assess the progression of bleeding. The study will also evaluate the effectiveness of different strategies to reverse the effects of P2Y12 inhibitors. A placebo is not used in this study.
Updated on 19 Feb 2024. Study ID: 1802316415

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