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Hypertension clinical trials

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NCT ID: NCT03630211 Not yet recruiting - Clinical trials for Pulmonary Hypertension

Autologous Stem Cell Transplantation in Patients With Systemic Sclerosis

SSc
Start date: August 2018
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether a regimen of high-dose immunoablative therapy will demonstrate safety that is consistent or improved with other published regimens in SSc patients, while maintaining a treatment effect. We also hypothesize that our mechanistic studies will yield biomarkers that may herald disease recurrence or progression following alterations in the recovery of immune cells in the skin and/or bronchial lavage or blood.

NCT ID: NCT03629912 Recruiting - Hypertension Clinical Trials

Bingocize: A Novel Mobile Application for Older Adult Health

Bingocize
Start date: August 14, 2018
Phase: N/A
Study type: Interventional

This study tests the effectiveness of using a new mobile application (Bingocize®) to improve older adults' (a) adherence to an engaging exercise program, and (b) aspects of functional performance, health knowledge, dietary habits, and cognition.

NCT ID: NCT03629535 Not yet recruiting - Hypertension Clinical Trials

Accuracy of Non-invasive Non-oscillometric Blood Pressure Wristband

Start date: October 2018
Phase: N/A
Study type: Interventional

The primary objective of the present investigation is to determine the accuracy of a non-invasive non-oscillometric blood pressure wristband device when compared to invasive intra-arterial blood pressure monitors. In an intensive care unit patients who already have an intra-arterial blood pressure monitor in place, this wristband device will be applied and blood pressure readings compared for approximately 15 minutes. Blood pressure readings will be gathered and compared.

NCT ID: NCT03629340 Not yet recruiting - Heart Failure Clinical Trials

Metformin for PH+HFpEF

Start date: September 2018
Phase: Phase 2
Study type: Interventional

The main objective of this study is to determine the clinical efficacy of metformin versus placebo and the therapeutic response with regards to functional capacity and hemodynamics in PH-HFpEF.

NCT ID: NCT03626688 Recruiting - Hypertension Clinical Trials

A Study Evaluating the Efficacy and Safety of Ralinepag to Improve Treatment Outcomes in PAH Patients

Start date: August 2018
Phase: Phase 3
Study type: Interventional

Study APD811-301, ADVANCE OUTCOMES, is designed to assess the efficacy and safety of ralinepag when added to pulmonary arterial hypertension (PAH) standard of care or PAH-specific background therapy in subjects with World Health Organization (WHO) Group 1 PAH.

NCT ID: NCT03626506 Not yet recruiting - Hypertension Clinical Trials

Spironolactone Versus Indapamide in Obese and Hypertensive Patients

Start date: August 2018
Phase: N/A
Study type: Interventional

Most recent guidelines continue to recommend thiazide diuretics as first-line agents for patients with hypertension in spite of the potential metabolic side effects, while mineralocorticoid receptor antagonists (MRAs), such as spironolactone or eplerenone, are mainly recommended to be used in patients with resistant hypertension or heart failure.However,animal studies demonstrated that MRAs induce beneficial changes in left ventricular remodeling and prevent or partially reverse cardiac fibrosis and pathological hypertrophy that contribute to the development of diastolic heart failure. MRAs have also been shown to decrease inflammation and myocardial fibrosis in patients with obesity and the metabolic syndrome. In the proposed study, we planned to randomize 400 patients with essential hypertension and increased waist circumference to receive spironolactone or indapamide in combination with amlodipine for 12 months. The effects of the two diuretics on target organ damage detected by changes in left atrial volume index(LAVI) by echocardiography reflecting left ventricular diastolic dysfunction or changes in carotid-femoral pulse wave velocity(PWV) reflecting arterial stiffness will be compared. The potential role of MRAs as initial therapy for patients with essential hypertension and visceral obesity will be evaluated.

NCT ID: NCT03626363 Not yet recruiting - Clinical trials for Elevated Blood Pressure

Mindfulness and Neural Cardiovascular Control in Humans

Start date: August 2018
Phase: N/A
Study type: Interventional

This study evaluates the impact of mindfulness-based stress reduction (MBSR) on sympathetic nerve activity and arterial stiffness. The investigator's central hypothesis is that MBSR will reduce sympathetic activity and arterial stiffness.

NCT ID: NCT03626259 Recruiting - Clinical trials for Arterial Hypertension

Losartan/Amlodipine on Hemodynamics Parameters and Arterial Stiffness in Arterial Hypertension

Start date: August 6, 2018
Phase: Phase 4
Study type: Interventional

Systemic Arterial Hypertension (SAH) is a disease with a high prevalence in Mexico and worldwide. SAH is associated with an increase in cardiovascular morbidity and mortality, causing cardiovascular disease (CVD), heart failure (HF), chronic kidney disease (CKD). Several of the physiopathological mechanisms observed are the increase in cardiac output, central aortic pressure (CAP), pulse wave velocity (PWV) and peripheral vascular resistance (PVR), which leads to the generation of damage to the target organ. The identification not only of the peripheral arterial pressure, but also of these hemodynamic parameters and arterial stiffness would allow a better cardiovascular characterization of the patients. However, the variation of all these hemodynamic parameters and arterial stiffness during the 24 hours can vary from individual to individual by all known mechanisms involved in the regulation of blood pressure such as cortisol, central nervous system and the peripheral nervous system, as well as the renin angiotensin and aldosterone system, which are usually only measured in a single moment, can vary throughout the 24 hours. Generally, the choice of drug in a patient with SAH is based only on the values of blood pressure at the time of measurement and the figures of peripheral blood pressure. The use of oscillometric equipment such as the Mobil-O-Graph 24 allows us to know the hemodynamic and arterial stiffness behavior during 24 hours; therefore, this could favor the choice of the most appropriate antihypertensive drug, the dose and the administration time. The use of angiotensin II receptor antagonists (ARA II) At1 blockers as losartan and calcium channel blockers (CCB) as amlodipine have shown a reduction in CAP and peripheral blood pressure respectively in patients with SAH. The most prescribed drugs in health units worldwide are enalapril, amlodipine, losartan and atenolol. Of which the most used combination is losartan with amlodipine. There are no studies to date that allow us to identify the effect of the administration of losartan / amlodipine in fixed combination form on hemodynamic parameters and arterial stiffness in patients with SAH. Therefore, the objective of the present study is to evaluate the effect of this fixed combination versus losartan on hemodynamic and arterial stiffness parameters based on the behavior of these for 24 hours.

NCT ID: NCT03624010 Not yet recruiting - Clinical trials for Heart Failure With Normal Ejection Fraction

Open-Label Rollover Study of Levosimendan in PH-HFpEF Patients

Start date: October 2018
Phase: Phase 2
Study type: Interventional

PH-HFpEF patients will receive weekly open-label doses of levosimendan and be periodically evaluated for safety and effectiveness in extended use.

NCT ID: NCT03620227 Recruiting - Hypertension Clinical Trials

Effects of Beetroot Juice in Postmenopausal and Hypertensive

Start date: February 1, 2018
Phase: N/A
Study type: Interventional

The decrease in estrogen in postmenopausal women leads an increase in endocrine metabolic dysfunctions, such as changes in lipid profile and blood pressure. Thus, one of the alternatives for prevention and treatment is the practice of physical exercise associated with diet containing precursors of nitric oxide (NO), which is a potent vasodilator. Therefore, this study intends to verify if supplementation of beetroot juice changes the hemodynamic and salivary markers in postmenopausal and hypertensive women. Therefore, the intervention consists of 350ml of concentrated beetroot juice or placebo, which will be ingested in fasting. After 2 hours will be carried out a session of aerobic physical exercise in treadmill and blood pressure will be measured each 15 minutes for 90 minutes after the end of the session, in addition to the 24-hour measurement that will be performed by an ABPM device. Salivary samples will be held: before the juice ingest, right after exercise, 90 minutes after and 24 hours after the end of the exercise. With the development of this study, it is expected to find blood pressure reduction and normalization of the inflammatory profile through salivary samples, after the period of supplementation associated with physical exercise practice.