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Coronary Vasospasm clinical trials

View clinical trials related to Coronary Vasospasm.

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NCT ID: NCT01317329 Completed - Obesity Clinical Trials

"Reversibility of Cardiovascular Injury With CPAP Use: Mechanisms Involved"

Start date: March 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the factors that are associated with improved cardiovascular function with the use of CPAP therapy on subjects diagnosed with moderate to severe obstructive sleep apnea.

NCT ID: NCT01173029 Completed - Stroke Clinical Trials

Renin-angiotensin-aldosterone System Polymorphisms in Resistant Hypertension and Adverse Cardiovascular Events

GENHART
Start date: June 2001
Phase: N/A
Study type: Observational

Renin-angiotensin-aldosterone system (RAAS) polymorphisms influence 24h arterial pressure fluctuation. Resistant systemic arterial hypertension (RSAH) has an increased risk of end organ damage and unfavourable prognosis, whereas pseudo-RSAH usually respond favourably to drug therapy. To prospectively investigate, in subjects with RSAH in a tropical South American city: 1) Adverse cardiovascular events defined as fatal and non-fatal stroke or acute myocardial infarction (AMI); and 2) the association of RAAS polymorphisms and adverse cardiovascular events in this population. Study population: 212 hypertensives recruited from primary care assistance (time since first diagnosis of hypertension: 16.5±8.1 years) and without appropriate pressure control, between 2001 and 2006, corresponding to 0.48% of all hypertensives under care (18 new cases/year), 57±10 years old, 66% females. Under drug treatment schedule: three or more drugs including a diuretic. Ninety two randomly selected hypertensives basis had renin-angiotensin-aldosterone system genetic profile determined. Genetic assessment was carried out using a polymerase chain reaction assay amplification technique. The following single nucleotide polymorphisms were analyzed: renin (G1051A), angiotensinogen (M235T), angiotensin converting enzyme-ACE (I/D), angiotensin II type 1 receptor (A1166C), aldosterone synthase (C344T) and mineralocorticoid receptor (G3514C).

NCT ID: NCT01117025 Completed - Atrial Fibrillation Clinical Trials

Combined Treatment of Resistant Hypertension and Atrial Fibrillation

Start date: April 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is the comparative evaluation of systolic blood pressure (SBP) lowering, atrial fibrillation (AF) recurrence and clinical data in patients with paroxysmal/persistent AF and resistant hypertension, undergoing AF ablation alone or combined with percutaneous renal denervation.

NCT ID: NCT01062763 Completed - Diabetes Mellitus Clinical Trials

The Effect of Spironolactone on Blood Pressure in Type-2 Diabetics With Resistant Hypertension

SDHDS
Start date: March 2010
Phase: Phase 3
Study type: Interventional

The purpose of this study is to estimate the effect of spironolactone on blood pressure resistant to therapy in type-2 diabetics.

NCT ID: NCT00619294 Completed - Coronary Vasospasm Clinical Trials

Endothelial Dysfunction and Coronary Artery Spasm

Start date: August 2006
Phase: N/A
Study type: Observational

Non-obstructive coronary artery disease (NOCAD) frequently accounts for myocardial ischemia in women. Endothelial dysfunction is a pathogenic factor in coronary spastic angina (CSA). CSA is an important cause of NOCAD diagnosed invasively by coronary angiography (CAG). Digital reactive hyperemia peripheral arterial tonometry (RH-PAT) provides noninvasive evaluation of endothelial dysfunction. The investigators hypothesized that the fingertip RH-PAT could predict the presence of CSA in women.

NCT ID: NCT00350129 Completed - Coronary Vasospasm Clinical Trials

Effect of Glucose on Ocular Blood Flow

Start date: December 2002
Phase:
Study type: Observational

The primary objective is to assess the effect of glucose on retinal vascular diameter in otherwise healthy vasospastic subjects compared to non-vasospastic controls. The secondary objective is to compare the effect of glucose also on choroidal blood flow in otherwise healthy vasospastic subjects with non-vasospastic controls.