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NCT Number: NCT07364058

Assessment of Platelet-derived GARP in Atherosclerotic Disease

The leading cause of death is cardiovascular diseases in occidental countries. Of those, atherosclerosis is the major contributor to this burden being notably responsible for strokes and myocardial infarctions. The genesis of atherosclerosis is linked to both lipid accumulation and inflammation in the vascular wall of major arteries. One of the major pathways of inflammation is the TGF-beta axis which is at least partially regulated by the GARP protein. It has been investigated mostly in cancer biology but data in cardiovascular disease is lacking. Thus, the investigators aim to characterize the contribution of this protein by investigating its expression in tissue from patients with atherosclerosis, the carotid or femoral plaque representing a good source of residual material adequate for research purpose. The main cells expressing the GARP protein are the platelets and the T regulating cells which will be the main focus.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Cliniques Universitaires Saint-Luc

Brussels, 1200, Belgium

Location contact

Christophe Beauloye, Medical Degree

PRINCIPAL_INVESTIGATOR

Louis Charki, Medical Degree

CONTACT

[email protected]

+3224362014

Louis Charki, Medical Degree

SUB_INVESTIGATOR

Maxime Elens, Medical Degree

SUB_INVESTIGATOR

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Older than 18 years
  • Able to give informed consent
  • Undergoing carotid or femoral endarterectomy

Exclusion criteria

  • Younger than 18 years
  • Pregnant
  • Dialysis
  • Unable to give informed consent

Treatment and study plan

Tissue sample and data collection

Other

Tissue sample and data collection

Primary outcomes

  1. GARP Expression in Platelets

    Time frame: Throughout the entire study, approximately during 3 years

    The number of cells/area expressing the GARP protein will be assessed

Secondary outcomes

  1. GARP Expression T Regulating Cells

    Time frame: Throughout the entire study, approximately during 3 years

    The number of cells expressing GARP will be assessed as a number of cells / area

  2. GARP Expression General

    Time frame: Throughout the entire study, approximately during 3 years

    The type of cells expressing GARP will be assessed as a number of cells / area

Study contacts

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

Louis Charki, Medical Degree

CONTACT

[email protected]

+3224362014

Sponsors and collaborators

Lead sponsor

Université Catholique de Louvain

Other

Collaborators

  • Fonds National de la Recherche Scientifique

Registry information

Acronym: CAPGAD

Important dates

Study start
2026
Primary completion
2029
Study completion
2029
First posted
Jan 23, 2026
Registry last updated
Jan 27, 2026

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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