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Completed

NCT Number: NCT04342819

The Effect of empagliFlozin on Platelet Function profilEs in diabetiC patienTs - The EFFECT Study.

The mechanistic effects of empagliflozin on platelet function profiles have not yet been ascertained.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Eric Williams Medical Sciences Complex

Port of Spain, North, 00000, Trinidad and Tobago

About this study

Sodium GLucose Transport 2 inhibitors (SGLT2I), including empagliflozin, reduce the likelihood of hospitalization for heart failure and death in persons with type 2 diabetes, of which the mechanism has not been fully elucidated. The mechanistic effects of empagliflozin on platelet function profiles have not yet been ascertained. It remains unclear if this reduction in cardiovascular death is mediated by decreased platelet reactivity.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • between 18 and 74 years of age,
  • have stable coronary artery disease and diabetes mellitus, already on DAPT with aspirin and clopidogrel for at least 6 months,

Exclusion criteria

  • presence of active internal bleeding or history of bleeding diathesis or clinical findings associated with an increased risk of bleeding,
  • history of ischemic or hemorrhagic stroke, transient ischemic attack, intracranial neoplasm, arteriovenous malformation, or aneurysm,
  • history of clinical and/or hemodynamic instability,
  • within 1 month of placement of a bare metal stent,
  • within 30 days of coronary artery bypass graft surgery or PCI without a stent placed,
  • planned coronary revascularization,
  • treatment with fibrin-specific fibrinolytic therapy <24 h or non-fibrin-specific fibrinolytic therapy <48 h,
  • use of an oral anticoagulation agent or international normalized ratio >1.5,
  • body weight <60 kg,
  • age >75 years,
  • hemoglobin <10 g/dL,
  • platelet count <100×106/μL,
  • creatinine >2 mg/dL,
  • hepatic enzymes >2.5 times the upper limit of normal,
  • pregnancy and/or lactation.

Treatment and study plan

SGLT2 inhibitor

Drug

Sodium-Glucose Like Transporter 2 Inhibitor

Other names: Empagliflozin

Primary outcomes

  1. P2Y12 Reaction Units

    Time frame: 14 days

    P2Y12 Reaction Units post-Empagliflozin. Citrated blood samples are processed by CRAs and study investigators. The platelet function assay to be utilized is the VerifyNow P2Y12 (VN-P2Y12) assay (Accriva, San Diego, California). In brief, the VN-P2Y12 assay is a rapid whole blood point-of-care device that reports results as P2Y12 reaction units (PRU) and percent inhibition of platelet aggregation (%IPA). Assays will be performed as per the instructions of the manufacturer previously described.

Sponsors and collaborators

Lead sponsor

The University of The West Indies

Other

Registry information

Acronym: EFFECT

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
Apr 13, 2020
Registry last updated
Sep 3, 2024

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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