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Hypertension clinical trials

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NCT ID: NCT03598673 Recruiting - Hypertension Clinical Trials

To Determine the Effect of Nebivolol on Office Blood Pressure of Blacks Residing in Nigeria

Start date: February 27, 2018
Study type: Observational

Although Nebivolol, a highly selective beta-1 agent has been shown to be effective in reducing blood pressure in Blacks, this was in African Americans with no study in Blacks residing in sub Saharan Africa. We therefore decided to study the effectiveness and safety of Nebivolol in Black patients with stage 1 hypertension (systolic BP of 140-149 and/or diastolic BP of 90-99 mmHg) presenting to five primary care centres in Nigeria.

NCT ID: NCT03590860 Recruiting - Hypertension Clinical Trials

A Study of LY3322207 in Healthy Participants and in Participants With Hypertension (High Blood Pressure)

Start date: July 13, 2018
Phase: Phase 1
Study type: Interventional

The purpose of this study is to investigate the safety of the study drug known as LY3322207. Participants must be healthy or must have hypertension (high blood pressure). Participants with hypertension may already be taking a common drug to reduce blood pressure called an angiotensin-converting enzyme inhibitor (ACE-I) or an angiotensin II receptor blocker (ARB).

NCT ID: NCT03588520 Recruiting - Hypertension Clinical Trials

Home Blood Pressure (HBP)-Guided Management of Hypertension in Stage 3-4 CKD

Start date: June 2, 2018
Phase: N/A
Study type: Interventional

It is estimated that over 25% of the world's population had hypertension in the year 2000 and that this proportion will reach 30% in the year 2025. With the introduction of the 2017 Guideline for High Blood Pressure in Adults from the American College of Cardiology and the American Heart Association Task Force on Clinical Practice Guidelines, the definition of hypertension became broader and as a result the prevalence is expected to further increase. On the other hand, it is estimated that around 10% of the world's population is affected by chronic kidney disease (CKD) with hypertension being both cause and complication of CKD. It is obvious that hypertension and CKD are interconnected and are both major risk factors for cardiovascular disease (CVD). Hypertension results in increased CVD risk both directly, as an independent factor, and indirectly via its negative impact on renal function. In fact, the deterioration of the renal function is proportional to the degree of hypertension. On the other hand, the more advanced the CKD is, the more challenging the management of hypertension becomes, as patients with CKD present altered patterns of blood pressure (BP) during the day and, additionally, the prevalence of white coat and masked hypertension is significantly higher in this group of patients. To date, hypertensive patients are treated according to the BP recordings that are obtained in the office (OBP) during routine patient visits, which leads to inaccurate estimates of the true burden of hypertension and also affects the efficacy of the therapeutic intervention. It has been suggested that self measured BP (HBP) is a more accurate estimate of the patients' daytime BP compared to the conventional office BP measurements. This has been already confirmed in studies regarding the general population and it has been suggested that the same applies to the patients with CKD. This study aims to check the validity of this hypothesis by comparing the effect of the HBP - guided management versus the conventional OBP - guided management on the 24 hour ambulatory BP monitoring of patients with uncontrolled hypertension and CKD stage 3 and 4.

NCT ID: NCT03586037 Recruiting - Hypertension Clinical Trials

Evaluating the Pharmacokinetic Interaction Between AD-2011 and AD-2012

Start date: June 12, 2018
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the Pharmacokinetic Interaction Between AD-2011 and AD-2012 in healthy male volunteers.

NCT ID: NCT03584607 Recruiting - Insulin Resistance Clinical Trials

Insulin- and Glucose Metabolism in Pulmonary Arterial Hypertension

Start date: December 20, 2017
Study type: Observational

Insulin resistance is a key mechanism in metabolic disorders, which has also been implicated in the development of pulmonary hypertension. In this pilot study, the investigators´ goal is to directly determine insulin sensitivity in idiopathic pulmonary arterial hypertension patients and to compare the results with data from healthy controls.

NCT ID: NCT03583866 Recruiting - Hypertension Clinical Trials

Adiposity and Endothelin Receptor Function

Start date: May 21, 2018
Phase: Early Phase 1
Study type: Interventional

Elevated levels of ET-1 have been implicated in cardiovascular disease and some forms of hypertension. Due to the strong, positive correlation between obesity and hypertension, the present study will explore the contribution of adiposity in ETB receptor function and aim to elucidate if ETB receptor dysfunction is a major contributor to hypertension in obesity.

NCT ID: NCT03581695 Recruiting - Clinical trials for Hypertension, Pulmonary

Inflammatory Biomarkers of Pediatric Pulmonary Hypertension

Start date: June 20, 2018
Study type: Observational

To investigate if the inflammatory protein, high mobility group box 1 (HMGB1), along with other inflammatory mediators, is elevated in pediatric patients with congenital heart disease (CHD) and pulmonary hypertension as compared to those with CHD alone, or with healthy controls.

NCT ID: NCT03579862 Recruiting - Clinical trials for Chronic Thromboembolic Pulmonary Hypertension

Identification of Heritable CTEPH

Start date: December 25, 2013
Study type: Observational

Some patients who have blood clots come down with a life-threatening condition known as Chronic Thromboembolic Pulmonary Hypertension (CTEPH), which is high blood pressure only in the arteries of the lungs. This study seeks to understand more about the genetics causes of CTEPH by obtaining blood samples and examining family histories.

NCT ID: NCT03579108 Recruiting - Hypertension Clinical Trials

Hypertension Management in Family Practice

Start date: February 24, 2018
Study type: Observational

High blood pressure is the greatest threat to the global burden of disease, contributing to an estimated 9.4 million deaths a year. Cardiovascular disease morbidity and mortality are positively correlated with the degree of elevation of blood pressure, without any evidence of a threshold down to at least 115/75 mm Hg[2]. Hypertension is common, and nearly every clinician in every specialty deals either directly or indirectly with managing it or its consequences. The population age 65 years or older numbered 46.2 million in 2014 and they represent 14.5% of the US population, the older population in 2030 is projected to be more than twice as large as in 2000, growing from 35 million to 74 million and representing 21 percent of the total U.S. population and it is expected to more than double to 98 million in 2060.Proper managing and controlling blood pressure markedly improves patient morbidity and mortality, SHEP study showed that in persons aged 60 years and over with isolated systolic hypertension, antihypertensive stepped-care drug treatment with low-dose chlorthalidone as step 1 medication reduced the incidence of total stroke by 36%.This study will estimate the prevalence of hypertension diagnosis, treatment and outcomes in a Family Practice population. It is a hypothesis generating study

NCT ID: NCT03578848 Recruiting - Hypertension Clinical Trials

Guiding Hypertension Management Using Different Blood Pressure Monitoring Strategies

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

Patients with uncontrolled or newly diagnosed hypertension will be randomized to have hypertension management decisions made on the basis of the unattended automated blood pressure (uAOBP) , home BP, and central BP monitoring. This study evaluates the optimal guiding strategy for hypertension will help define which BP monitoring is the most effective strategy to guide the clinical management of hypertension.