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Atherosclerosis clinical trials

View clinical trials related to Atherosclerosis.

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NCT ID: NCT01747525 Withdrawn - Clinical trials for Coronary Artery Disease

Near-Infrared Spectroscopy and Ultrasound Investigation of Coronary Artery Plaque

LUNAR
Start date: October 2011
Phase: N/A
Study type: Observational

The primary objective of this study is to characterize coronary artery blockages as determined by the LipiScan combined NIRS-IVUS catheter using multi-vessel imaging.

NCT ID: NCT01745458 Completed - Atherosclerosis Clinical Trials

SB-659032 Platelet Aggregation Study

Start date: July 2005
Phase: Phase 1
Study type: Interventional

This study is designed to assess whether inhibition of plasma Lp-PLA2 activity impacts platelet function as assessed by ex vivo platelet aggregation tests and in vivo plasma biomarkers.

NCT ID: NCT01743404 Recruiting - Clinical trials for Carotid Atherosclerosis

Study of Anti-atherosclerotic Activity of Inflaminat in Asymptomatic Participants With Subclinical Atherosclerosis

Start date: September 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to investigate the anti-atherosclerotic effect of long-term anti-inflammatory therapy (Inflaminat) in asymptomatic participants with subclinical atherosclerosis of carotid arteries.

NCT ID: NCT01742845 Completed - Clinical trials for Carotid Atherosclerosis

Ultrasound-guided Intermediate Cervical Block Versus Superficial Cervical Block for Carotid Endarterectomy (CERVECHO)

CERVECHO
Start date: April 2011
Phase: N/A
Study type: Interventional

The aim of this prospective, randomised, controlled study is to compare the efficacy of ultrasound-guided intermediate cervical block to superficial block for carotid endarterectomy. Patients scheduled for carotide endarterectomy under regional anaesthesia (ropivacaine 4.75 mg/ml) are randomised into 2 groups according to the technique of anaesthesia performed: superficial cervical block (Control group) or, ultrasound guided intermediate cervical block (Echo group). Main outcome is cervical block success, defined by surgery performed under regional anaesthesia without supplemental topical lidocaine. Secondary outcomes are rate of conversion to general anaesthesia, total dose of supplemental topical lidocaine and block-related complications.

NCT ID: NCT01742000 Completed - Atherosclerosis Clinical Trials

Study of Anti-atherosclerotic Activity of Karinat in Postmenopausal Women

PEARS-POST
Start date: January 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to investigate the anti-atherosclerotic action of natural drug Karinat based on phytoestrogen-rich botanicals in postmenopausal women.

NCT ID: NCT01741974 Completed - Atherosclerosis Clinical Trials

Study of Anti-atherosclerotic and Estrogen-like Activity of Karinat in Perimenopausal Women

PEARS
Start date: October 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study is to investigate the anti-atherosclerotic and anti-climacteric action of natural drug Karinat based on phytoestrogen-rich botanicals in perimenopausal women.

NCT ID: NCT01734707 Completed - Clinical trials for Carotid Atherosclerosis

Atherosclerosis Monitoring and Atherogenicity Reduction Study

Start date: January 2004
Phase: Phase 3
Study type: Interventional

This study was designed to estimate the effect of two-year treatment with time-released garlic-based drug Allicor on the progression of carotid atherosclerosis in double-blinded placebo-controlled randomized clinical trial.

NCT ID: NCT01734629 Completed - Clinical trials for Coronary Artery Disease

Pulmonary Disease in Patients Referred for Coronary CT

Start date: April 2011
Phase: N/A
Study type: Observational

Several studies show an association between chronic obstructive pulmonary disease (COPD) and coronary artery disease (CAD). Besides risk factors such as smoking, both are associated with physical inactivity, advanced age and systemic inflammation The use of coronary computed tomography (CCT) with multiple detectors is a diagnostic method for coronary disease, describing the anatomy and severity of arterial obstruction. One way of estimating the cardiovascular risk is coronary calcium score (CCS). Due to the association between COPD and CAD, it is likely that many patients with IHD diagnosed by CT have reduced lung function. The aim of this observational study is to establish the correlation between the CCS and lung function. It will also correlate the presence of irreversible airway obstruction with significant coronary lesions. Patients over 40 years referred to CCT who agree to participate in the study will perform a spirometry with bronchodilator and collect a blood sample to measure serum markers of inflammation and cardiovascular risk (glycemia, lipid profile, C reactive protein (CRP), tumor necrosis factor-alpha (TNF-Alpha) and fibrinogen). The data will be compared in the general population and in subgroups: smokers, former smokers and nonsmokers. One year after the CCT patients will be contacted by the investigators and accessed for emergency room visits, hospital admissions and fatal or nonfatal coronary or respiratory events. The investigators hypothesis is that reduced lung function is independently associated with elevated CCS and is, also a risk factor for increased hospital admission and coronary events. The concomitant assessment of lung function and CCS can contribute knowledge about the epidemiological association between pulmonary disease and CAD. This can also add to evidence for the use of spirometry as a marker of cardiovascular risk.

NCT ID: NCT01724749 Recruiting - Clinical trials for Cardiovascular Disease

Cardiovascular Molecular Calcification Assessed by 18F-NaF PET CT

CAMONA
Start date: November 2012
Phase: N/A
Study type: Observational

The purpose of the CAMONA study is to demonstrate the feasibility of cardiovascular molecular calcification (CMC) assessment by means of 18F-sodium-fluoride (18F-NaF) positron emission tomography (PET) computed tomography (CT) in a prospective cohort of healthy control subjects and subjects with cardiovascular disease.

NCT ID: NCT01722214 Completed - Psoriasis Clinical Trials

Trial on the Effect of Adalimumab on Vascular Inflammation in Patients With Psoriasis

Start date: November 2012
Phase: Phase 4
Study type: Interventional

This study is a double-blinded randomized multicenter placebo controlled trial to determine the effect of adalimumab on vascular inflammation (ascending aorta and carotides) in patients with moderate to severe psoriasis.