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Physical,Histological,and Genetic Analyses of Lipid-rich Atherosclerotic Plaques

Physical,Histological,and Genetic Analyses of Lipid-rich Atherosclerotic Plaques

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00449306
Enrollment
120
Registered
2007-03-20
Start date
2001-03-31
Completion date
2021-07-31
Last updated
2019-07-05

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

Conditions

Aortic Aneurysm, Atherosclerosis, Peripheral Vascular Diseases

Keywords

Atherosclerosis, Carotid plaque, Abdominal aortic aneurysm, Vulnerable plaque, Angiogenesis, Intraplaque hemorrhage, Carotid artery atherosclerosis

Brief summary

Lipid-rich atherosclerotic plaques, or vulnerable plaques are prone to rupture, causing local intravascular thrombosis, with subsequent grave clinical consequences. Atherosclerotic plaques normally removed during surgery, and peripheral blood samples will be studied to achieve the following objectives: 1 Define histological features of the vulnerable plaque, analyze its physical characteristics, and investigate selected gene expression. 2 Study biomarkers of inflammation in conjunction with the presence of vulnerable plaques. 3 Explore the potential role of infection in atherogenesis.

Interventions

None listed

Sponsors

University Hospital Goettingen
CollaboratorOTHER
Carmel Medical Center
CollaboratorOTHER
CVPath Institute Inc.
CollaboratorOTHER
Sheba Medical Center
Lead SponsorOTHER_GOV

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

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

Inclusion criteria

* Evidence of symptomatic carotid stenosis exceeding 60%(TIAs or stroke within the last 6 months), and asymptomatic carotid artery stenosis (presenting with progressive carotid stenosis, exceeding 70%) * Abdominal aortic aneurysm, and aortic occlusive disease * Peripheral occlusive or aneurysmal disease

Exclusion criteria

* Non-compliant patients, incapable of granting approval by informed consent

Design outcomes

Primary

MeasureTime frame
To uncover mechanisms of cardiovascular diseases3 years

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 25, 2026