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NCT Number: NCT07169513

Mechanistic Study of Anti-Platelet Therapy in Atherosclerosis

Many people have a higher chance of getting heart problems. These individuals include people who are very overweight (obesity), have high blood pressure (hypertension), diabetes, or other health concerns. Heart problems often happen because of a condition called atherosclerosis. This condition is when the arteries, which are the blood vessels carrying blood from the heart, become hard and inflamed (swollen and irritated) at the same time. Atherosclerosis causes arteries narrowing, making it harder for blood to flow through. The signs of atherosclerosis can be mild, like feeling chest pain (called angina) because the heart isn't getting enough blood. In more serious cases, it can lead to a heart attack.

Think of inflammation as the body's natural alarm system. When a person gets hurt or sick, the body releases special chemicals. These chemicals tell the immune system (the body's defence team) to come and help. Their job is to heal the injury or fight off the infection.

While inflammation is usually good, sometimes it can go wrong. Atherosclerosis is one of these conditions where the inflammation in the blood vessels becomes abnormal. This ongoing inflammation can harm the body and lead to various heart problems and other health issues not directly related to the heart.

In atherosclerosis, platelets (cell fragments in our blood that form clots and stop or prevent bleeding) bind to monocytes (a type of white blood cell and a type of phagocyte - part of the immune system) to form clusters called monocyte platelet aggregate (MPA). Studies have shown that people with atherosclerosis have higher levels of the monocytes clustering with the platelets. This aggregate contributes to the worsening of atherosclerosis. Additionally, this aggregate can predict the risk of developing various cardiac diseases.

Anti-platelet (anti-clotting) medications work by stopping platelet function. In this study, investigators are giving participants two different anti-platelet medications to study the effect of these medications on the level of MPA. The target people of our study are the people with silent atherosclerosis (there is an accumulation of lipids in the blood vessels but no signs or symptoms). No existing research demonstrates whether the two most commonly prescribed anti-platelets (aspirin and clopidogrel) can help reduce MPA levels. This study aims to show the effect of anti-platelet medications on the level of MPA and other inflammatory indicators. The two medications are aspirin and clopidogrel. These two drugs are already available in the market and widely used by different patients for different reasons. Aspirin and clopidogrel have different modes of action to stop platelet function.

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Key information

Conditions

Peripheral Arterial Disease Arterial Occlusive Diseases Arteriosclerosis Atherosclerosis Cardiovascular Diseases Peripheral Vascular Diseases Silent Atherosclerosis Vascular Diseases

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

Group 1:

  • Male or female age 18 years or older
  • Willing to participate in the study, and able to give informed consent
  • Negative pregnancy test for a childbearing age woman
  • Receiving standard of care
  • Confirmed atherosclerotic cardiovascular risk based on clinical assessment

Group 2:

  • Male or female age 18 years or older
  • Willing to participate in the study, and able to give informed consent
  • Receiving standard of care
  • Negative pregnancy test for a childbearing age woman
  • Confirmed diagnosis of peripheral arterial disease (ankle-brachial index below 0.9) with Rutherford grade 1-3.

Exclusion criteria

Group 1:

  • Diabetes
  • Receiving any anti-platelet medications within the last two weeks
  • Receiving any anticoagulant medications within the last two weeks
  • Receiving statin medications within the last two weeks
  • Known major organ dysfunction
  • Significant co-morbidities
  • Pregnancy or lactating woman
  • Unwilling, or unable to give informed consent
  • Presence of co-existing autoimmune disease
  • Hypersensitivity to aspirin or clopidogrel
  • Severe hepatic impairment (Child-Pugh grade C)
  • Active peptic ulcer
  • Presence of co-existing inflammatory or autoimmune diseases
  • Frequent use of medications known to affect platelet function five days before baseline phlebotomy and during the study
  • Non-steroidal anti-inflammatory drugs (NSAIDs)
  • Antihistamines
  • Selective serotonin reuptake inhibitors
  • Platelet count < 100 × 109 /L or > 450 × 109 /L
  • Anaemia
  • Any known bleeding diathesis
  • Currently involved in other clinical research studies

Group 2:

  • Diabetes
  • Patients with PAD Rutherford category of more than 3
  • Receiving any anticoagulant medications within the last two weeks
  • Known major organ dysfunction
  • Pregnancy or lactating woman
  • Unwilling, or unable, to give informed consent
  • Hypersensitivity to aspirin or clopidogrel
  • Severe hepatic impairment (Child-Pugh grade C)
  • Active peptic ulcer
  • Presence of co-existing autoimmune disease
  • Frequent use of medications known to affect platelet function five days before baseline phlebotomy and during the study
  • Non-steroidal anti-inflammatory drugs (NSAIDs)
  • Antihistamines
  • Selective serotonin reuptake inhibitors
  • Platelet count < 100 × 109 /L or > 450 × 109 /L
  • Anaemia
  • Any known bleeding diathesis
  • Currently involved in other clinical research studies

Treatment and study plan

Aspirin 75 mg daily

Drug

For group 1 patients

Clopidogrel 75 mg daily

Drug

For group 2 patients

Clopidgrel 75 mg daily

Drug

For group 1 patients

Aspirin 75 mg daily + Clopidgrel 75 mg daily

Drug

For group 2 patients

Primary outcomes

  1. Monocyte-platelet aggregates (MPAs)

    Time frame: Maximum 14 weeks

    Changes in the percentages of monocyte-platelet aggregates (MPAs) in two groups of patients following treatment with aspirin and clopidogrel using flow cytometry

Secondary outcomes

  1. Monocyte and platelet activation/phenotype

    Time frame: Maximum 14 weeks

    Measure the effect of aspirin, clopidogrel, and their combination on monocyte and platelet activation/phenotype using flow cytometry

  2. Circulating mediators of inflammation

    Time frame: Maximum 14 weeks

    Measure the influence of aspirin, clopidogrel, and their combination on the level of circulating mediators of inflammation using multiplex Luminex assay

  3. Gene expression

    Time frame: Maximum 14 weeks

    Determine how aspirin, clopidogrel, and their combination modulate gene expression using single-cell RNA sequencing

Study contacts

Contact information is provided by the study sponsor or research team.

Ashish Patel

CONTACT

[email protected]

0442071880216

Eman Al Musalami

CONTACT

[email protected]

Sponsors and collaborators

Lead sponsor

Guy's and St Thomas' NHS Foundation Trust

Other

Collaborators

  • King's College London

Registry information

Official study title

Targeting the Inflammasome With Anti-platelet Therapy: A Mechanistic Study

Acronym: MPA

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Sep 11, 2025
Registry last updated
Sep 11, 2025

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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