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Completed

NCT Number: NCT03774394

Impact of Chronic Kidney Disease on Clopidogrel Effects in Diabetes Mellitus

Patients with diabetes mellitus (DM) and chronic kidney disease (CKD) are at increased risk of atherothrombotic events. Clopidogrel is the most widely used platelet P2Y12 receptor inhibitor in patients with coronary artery disease (CAD). However, despite its benefits, many patients still experience recurrent atherothrombotic events. The proposed study will test the central hypothesis that in DM patients the presence of CKD reduces clopidogrel-mediated P2Y12 inhibitory effects through synergistic mechanisms, which include upregulation of the P2Y12 signaling pathway and impaired clopidogrel metabolism.

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Key information

About this study

Patients with diabetes mellitus (DM) and coexisting chronic kidney disease (CKD) are at increased risk of atherothrombotic events, underscoring the importance of secondary prevention antiplatelet therapy in these high-risk patients. Clopidogrel is the most widely used platelet P2Y12 receptor inhibitor in patients with coronary artery disease (CAD). However, despite its clinical benefits, many patients still experience recurrent atherothrombotic events. This is in part due to the impaired effects of clopidogrel in DM patients, particularly among those with coexisting CKD. However, underlying mechanism(s) leading to magnification of impaired clopidogrel response among DM patients with CKD remain unexplored. The ever growing prevalence of CKD in patients with DM and their high risk of recurrent events underscores the need to define such mechanism(s) as this may set the basis for identifying treatment regimens leading to more effective platelet inhibition and cardiovascular protection in these high-risk patients. The proposed study will test the central hypothesis that in DM patients the presence of CKD reduces clopidogrel-mediated P2Y12 inhibitory effects through synergistic mechanisms, which include upregulation of the P2Y12 signaling pathway and impaired clopidogrel metabolism. Comprehensive pharmacokinetic and pharmacodynamic assessments, including ex vivo and in vitro experiments, evaluating the impact of CKD on antiplatelet drug response in DM patients are proposed.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Type 2 DM, defined according to ADA definition, on treatment with oral hypoglycemic agents and/or insulin
  • Angiographically documented CAD
  • On treatment with low-dose aspirin (81mg/day) for ≥30 days as part of standard of care.

Exclusion criteria

  • Use of any antiplatelet therapy (except aspirin) in prior 30 days
  • Use of parenteral or oral anticoagulation
  • Active bleeding
  • High risk of bleeding
  • Clinical indication to be on a P2Y12 receptor inhibitor
  • End-stage renal disease on hemodialysis
  • Any active malignancy
  • Platelet count < 100x106/µl
  • Hemoglobin <9 g/dl
  • Severe known liver disease
  • Hemodynamic instability
  • Known allergy to clopidogrel
  • Pregnant / lactating females (women of childbearing age must use reliable birth control).

Treatment and study plan

clopidogrel

Drug

Both CKD and Non-CKD patients will be administered a 600-mg LD of clopidogrel followed by a single 75-mg MD administered after 24 hours.

Other names: Plavix

Clopidogrel active metabolite

Drug

In both CKD and Non-CKD patients, blood samples collected at baseline only (before clopidogrel LD administration) will be incubated with escalating concentrations of clopidogrel active metabolite (1, 3 and 10 μM)

Other names: Plavix

Primary outcomes

  1. Platelet Reactivity Index (PRI) Assessed by VASP. The Cutoff for High Platelet Reactivity is >50%

    Time frame: 6 hours

    Comparison of platelet reactivity measured as PRI assessed by VASP after a 600 mg clopidogrel LD between DM patients with and without CKD

Secondary outcomes

  1. Clopidogrel Active Metabolite Concentration

    Time frame: 6 hours

    Comparison of clopidogrel active metabolite plasma concentrations by means of AUC

Other outcomes

  1. P2Y12 Reaction Units (PRU) Assessed by VerifyNow. The Cutoff for High Platelet Reactivity is >208.

    Time frame: 6 hours

    Comparison of platelet reactivity measured as PRU assessed by VerifyNow after a 600 mg clopidogrel LD between DM patients with and without CKD

  2. Platelet Reactivity Index (PRI) Assessed by VASP. The Cutoff for High Platelet Reactivity is >50%

    Time frame: Baseline

    Comparison of of platelet reactivity measured as PRI assessed by VASP after incubation with clopidogrel active metabolite between DM patients with and without CKD

Sponsors and collaborators

Lead sponsor

University of Florida

Other

Collaborators

  • Scott R. MacKenzie Foundation

Registry information

Official study title

Impact of Chronic Kidney Disease (CKD) on Pharmacodynamic Profiles of the P2Y12 Receptor Inhibitor Clopidogrel in the Setting of Type 2 Diabetes Mellitus (T2DM) and Coronary Artery Disease (CAD)

Important dates

Study start
2019
Primary completion
2022
Study completion
2022
First posted
Dec 13, 2018
Registry last updated
Aug 21, 2023

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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