Clinical Trials Directory

Trials / Completed

CompletedNCT01678521

Effect of LDL-apheresis on PTX3 Plasma Levels in Hypercholesterolemic Patients

Effect of LDL-apheresis on Pentraxin3 Plasma Levels in Hypercholesterolemic Patients With Coronary Artery Disease

Status
Completed
Phase
Study type
Observational
Enrollment
12 (actual)
Sponsor
Universita di Verona · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Inflammation plays a major role in atherosclerosis. Pentraxin 3 (PTX3) a multifunctional pattern-recognition protein, is expressed in many tissues/cells, including innate immunity cells, endothelium and atherosclerotic plaques. Its role is controversial: it may exert protective cardiovascular effects and/or it may be an indicator of plaque vulnerability and future cardiovascular risk. LDL-Apheresis removes apoB100-containing lipoproteins and it can prevent progression of coronary artery disease (CAD). LDL-Apheresis exerts non-lipidic beneficial effects on the procoagulatory state and on hemorheology. No data exist about the effects of LDL-Apheresis on plasma PTX3 levels.

Detailed description

Hypercholesterolemic patients with documented CAD, on chronic fortnightly LDL-apheresis treatment will be enrolled in this study. Blood samples will be collected before and after a single LDL-Apheresis treatment to asses PTX3, HsCRP, IL6, IL10, Fibrinogen and lipid plasma levels.

Conditions

Interventions

TypeNameDescription
PROCEDURELDL-apheresisThe acronym H.E.L.P. stands for Heparin-induced Extracorporeal Low-density-lipoprotein Precipitation. Antecubital veins served as blood access. The mean blood volume processed per session is of approximately 3000 ml.

Timeline

Start date
2012-09-01
Primary completion
2013-12-01
Completion
2013-12-01
First posted
2012-09-05
Last updated
2014-12-19

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT01678521. Inclusion in this directory is not an endorsement.