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Hypertension clinical trials

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NCT ID: NCT02400775 Withdrawn - Clinical trials for Essential Hypertension With Stable Angina and Dyslipidemia

A Study to Evaluate the Effects of Azilsartan on Coronary Artery Plaque in Essential Hypertensive Patients With Stable Angina and Dyslipidemia.

ALIVE
Start date: March 2015
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the effects of oral azilsartan once daily for 32 weeks on coronary artery plaque in essential hypertensive patients with stable angina and dyslipidemia.

NCT ID: NCT02372721 Withdrawn - Hypertension Clinical Trials

Long Term Impact of Pediatric Acute Renal Injury in Severe Sepsis

IMPRESS
Start date: March 2015
Phase: N/A
Study type: Observational

Sepsis is the most common cause of childhood death worldwide. Millions of children survive, but are left with impaired health. Sepsis-related Acute Kidney Injury (sAKI) is increasingly recognized as a significant factor associated with long-term mortality among different patient populations. Renal dysfunction and subsequent chronic kidney disease is implicated in the development of hypertension and cardiovascular disease. The investigators overall hypothesis is that, in the pediatric population, sepsis-related AKI will have unrecognized, long-term consequences with regard to kidney function, endothelial function, blood pressure control, and overall health.

NCT ID: NCT02357017 Withdrawn - Hypertension Clinical Trials

Mechanisms of Refractory Hypertension (High and Low Salt Diet)

Start date: February 2015
Phase: N/A
Study type: Interventional

The purpose of the study is to test the hypothesis that persistent fluid retention and high sympathetic output contributes to the development of refractory hypertension (HTN). The investigators will determine, in a cross-over assessment of high and low salt diets, if dietary sodium restriction reduces 24-hr ambulatory BP in patients with refractory HTN. Moreover, the investigators will determine if dietary sodium restriction lessens the severity of obstructive sleep apnea (OSA) in patients with refractory HTN.

NCT ID: NCT02339961 Withdrawn - Clinical trials for Pulmonary Hypertension

Evaluating Pulmonary Arterial Hypertension in Patients With Systemic Sclerosis

Start date: February 2015
Phase: N/A
Study type: Interventional

Doppler signals can be recorded from the lung parenchyma by means of a pulsed Doppler ultrasound system incorporating a special signal processing package- the Transthoracic Parametric Doppler (TPD) (Echosense Ltd., Haifa, Israel). Systemic sclerosis patients often develop pulmonary vascular disease leading to pulmonary hypertension. The TPD system may provide important insight into pulmonary blood vessels characteristics by the LDS (Lung Doppler Signals) signals that are related to pulmonary hypertension. The TPD performance in detecting PAH in SSc patients will be assessed in the study.

NCT ID: NCT02309463 Withdrawn - Clinical trials for Pulmonary Arterial Hypertension

Correlation of LONGterm Wrist ACTigraphy Recorded Physical Performance & 6-minute Walk Distance in Patients With Pulmonary Arterial Hypertension

LONGACT
Start date: January 2015
Phase: N/A
Study type: Observational

The objective of the study is to monitor physical activity longitudinally with a wrist activity tracker specifically in PAH patients newly initiating ERA therapy and to assess the correlation with the 6MWD at different time points. Further objectives are to assess the correlation of physical activity measured with the tracker and other parameters for clinical evaluation and right ventricular function assessment (i.e. Biomarkers, WHO Functional class, hospitalization due to PAH, Echochardiography and Quality of Life) as well as sleep efficacy in PAH patients newly initiating ERA therapy.

NCT ID: NCT02278445 Withdrawn - Clinical trials for Pulmonary Hypertension

Evaluation of Pulmonary Doppler Signals in Patients With Systemic Sclerosis(SSc)

Start date: November 2014
Phase: N/A
Study type: Interventional

Doppler signals can be recorded from the lung parenchyma by means of a pulsed Doppler ultrasound system incorporating a special signal processing package- the Transthoracic Parametric Doppler (TPD) (Echosense Ltd., Haifa, Israel). Systemic sclerosis patients often develop pulmonary vascular disease leading to pulmonary hypertension. The TPD system may provide important insight into pulmonary blood vessels characteristics by the LDS (Lung Doppler Signals) signals that are related to pulmonary hypertension. The TPD performance in detecting PAH in SSc patients will be assessed in the study.

NCT ID: NCT02269072 Withdrawn - Hypertension Clinical Trials

Testosterone Regulation of the Natriuretic Peptide System

Start date: February 2015
Phase: N/A
Study type: Interventional

The proposed study is a physiologic investigation of the effects of testosterone on the natriuretic peptide system. The hypotheses of the study are that testosterone administration will decrease natriuretic peptide levels and salt excretion. The entire protocol is 8 weeks in duration.

NCT ID: NCT02217683 Withdrawn - Clinical trials for Hypertension, Pulmonary

Use of Inhaled Nitric Oxide to Prevent Pulmonary Hypertension Associated to Stored Blood Transfusion

Start date: March 2016
Phase: Phase 2
Study type: Interventional

The objective of this study is to assess if prolonged storage time of a packed red blood cell unit may cause pulmonary vasoconstriction after transfusion, in a susceptible population such as cardiac surgery patients. The investigators will also evaluate the potential reversal effect of Inhaled Nitric Oxide on pulmonary vasoconstriction induced by stored blood transfusions.

NCT ID: NCT02150382 Withdrawn - Hypertension Clinical Trials

China Rural Hypertension Control Project 2014

Start date: February 2014
Phase:
Study type: Observational

China Rural Hypertension Control (CRHC) Project is a cluster randomized trial aims to test the effectiveness of a standardized protocol-based treatment program on hypertension control in rural China.

NCT ID: NCT02138708 Withdrawn - Clinical trials for Pulmonary Arterial Hypertension With Congenital Cardiac Shunt

Evaluation of the Pulmonary Vascular Reactivity Test in Patients With Pulmonary Arterial Hypertension and a Cardiac Shunt

ReVAch
Start date: January 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the predictive performance of the pulmonary vascular reactivity to acetylcholine, in the presence pulmonary arterial hypertension (estimated 1 year after the closure of the shunt).