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Assessment of Platelet-derived GARP in Atherosclerotic Disease

Assessment of Platelet-derived GARP in Atherosclerotic Disease

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07364058
Acronym
CAPGAD
Enrollment
200
Registered
2026-01-23
Start date
2026-02-01
Completion date
2029-01-01
Last updated
2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atheroma; Carotid Artery, Atheromatosis

Keywords

Atheroma, Atherosclerosis, GARP, LRRC32

Brief summary

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.

Interventions

OTHERTissue sample and data collection

Tissue sample and data collection

Sponsors

Université Catholique de Louvain
Lead SponsorOTHER
Fonds National de la Recherche Scientifique
CollaboratorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
GARP Expression in PlateletsThroughout the entire study, approximately during 3 yearsThe number of cells/area expressing the GARP protein will be assessed

Secondary

MeasureTime frameDescription
GARP Expression T Regulating CellsThroughout the entire study, approximately during 3 yearsThe number of cells expressing GARP will be assessed as a number of cells / area
GARP Expression GeneralThroughout the entire study, approximately during 3 yearsThe type of cells expressing GARP will be assessed as a number of cells / area

Countries

Belgium

Contacts

CONTACTLouis Charki, Medical Degree
louis.charki@uclouvain.be+3224362014
PRINCIPAL_INVESTIGATORChristophe Beauloye, Medical Degree

Cliniques universitaires Saint-Luc- Université Catholique de Louvain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026