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Blood Pressure clinical trials

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NCT ID: NCT04579315 Completed - Blood Pressure Clinical Trials

Long-term Effects of the New Nordic Renal Diet in Patients With Moderate Chronic Kidney Disease

CKD
Start date: November 30, 2020
Phase: N/A
Study type: Interventional

As Chronic Kidney Disease (CKD) progresses normophosphatemia is maintained by increasing the per nephron urinary phosphorus excretion. Clinically, hyperphosphatemia is associated with high mortality, vascular calcification, endothelial dysfunction and progression of left ventricular hypertrophy. Currently the treatment of hyperphosphatemia is first being initiated in stage 5 and consists of dietetic guidance to avoid dietary phosphate and treatment with oral phosphate binders. However, studies have shown important side effects to phosphate binders in terms of progression of vascular calcifications. Therefore, it might be beneficial to start the dietetic treatment with a reduction of dietary phosphate earlier in the disease stage. The aim of this project is to develop a New Nordic Renal Diet (NNRD) for CKD patients' stage 3-4 and to examine the long-term effects in a period of 26-weeks. NNRD has a high content of vegetable foods, less animal products and more local food items with a lesser content of phosphorus.

NCT ID: NCT04576338 Active, not recruiting - Sleep Clinical Trials

"Neighborhood Disadvantage, Sleep and Vascular Health"

NDSVH
Start date: January 11, 2020
Phase:
Study type: Observational

The purpose of the study is to find out the effects of neighborhood disadvantage and sleep disparities contribute to racial disparities in cardiometabolic health and blood pressure in young adults.

NCT ID: NCT04575194 Recruiting - Obesity Clinical Trials

Study of the Cardiometabolic Effects of Obesity Pharmacotherapy

Start date: September 8, 2020
Phase: Phase 4
Study type: Interventional

The aim of the present study is to compare the efficacy of liraglutide vs. naltrexone/bupropion on metabolic and cardiovascular risk markers, weight loss, as well as the postprandial secretion of gastrointestinal hormones involved in hunger and satiety, after a test meal. The study will include 40 patients, who will further be divided into two treatment groups (20 patients on liraglutide vs. 20 patients on naltrexone/bupropion). The patients will be examined at baseline, 3 and 6 months after the treatment initiation.

NCT ID: NCT04573595 Completed - Blood Pressure Clinical Trials

Fresenius Noninvasive Blood Pressure Validation

BPM2
Start date: September 17, 2020
Phase: N/A
Study type: Interventional

The purpose of this study to collect blood pressure measurement values from the blood pressure measurement device on the Fresenius machine as compared to the standard method.

NCT ID: NCT04556422 Completed - Blood Pressure Clinical Trials

Comparison of Acute Sauna With Exercise and Sauna

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

Sauna bathing has been associated with a lower risk for cardiovascular disease (CVD) outcomes, improved vascular endothelial and cardiac function, reduced oxidative stress and lower blood pressure. Earlier studies conducted by the investigators have showed positive alterations of arterial stiffness and hemodynamics through sauna bathing. Some studies have sought to utilize sauna bathing as an intervention after exercise with promising and synergistic results, although the effects on populations with cardiovascular risk factors are less clear. Furthermore, studies investigating the use of both exercise and sauna bathing in combination has been somewhat limited. However, results from some studies speculate that adjunctive exercise and sauna interventions may be useful for aging and clinical patient population groups. Given that heat therapy and sauna use is gaining more worldwide popularity, the investigators sought to compare the acute hemodynamic effects between sauna use alone and a short bout of exercise followed by sauna exposure. It was hypothesize that the combination of exercise and sauna will elicit greater changes than sauna alone. To achieve this, we standardized the protocol duration (30 minutes).

NCT ID: NCT04553861 Completed - Blood Pressure Clinical Trials

Smartwatch ABPM vs. Conventional ABPM

SamsungWatch
Start date: November 1, 2020
Phase:
Study type: Observational [Patient Registry]

This study aims to investigate the accuracy and precision of the Samsung Smartwatch with conventional ambulatory blood pressure monitoring in healthy volunteers.

NCT ID: NCT04548986 Completed - Hypertension Clinical Trials

Single-center Prospective Study to Validate the Performance of the Aktiia Optical Blood Pressure Monitoring (OBPM) Device at the Wrist Against Ambulatory Blood Pressure Monitoring (ABPM)

OBPM_ABPM2020
Start date: August 6, 2020
Phase: N/A
Study type: Interventional

This study aims to assess the performances of optical blood pressure monitoring device, Aktiia.product in the context of cardiac rehabilitation program.

NCT ID: NCT04545034 Enrolling by invitation - Hypertension Clinical Trials

Water Aerobics Session on Blood Pressure of Hypertensive Elderly.

Start date: April 1, 2020
Phase: N/A
Study type: Interventional

This randomized controlled trial aimed to determine the subacute blood pressure effects of pharmacologically-treated elderly hypertensive patients after a single session of water aerobic exercise.

NCT ID: NCT04539860 Recruiting - Blood Pressure Clinical Trials

Comparison of Blood Pressure Measurements Between Transdermal Optical Imaging and Standard of Care

Start date: August 25, 2020
Phase:
Study type: Observational

Participants (patients and volunteers) will be recruited to have their blood pressure measured by standard blood pressure assessment methods while having their face video recorded. The data collected will help improve the blood pressure measurement accuracy of Transdermal Optical Imaging, which relies on machine learning to extract physiological information from videos recorded.

NCT ID: NCT04524325 Withdrawn - Blood Pressure Clinical Trials

Mechanisms of Blood Pressure Dysfunction in Transmen Receiving Testosterone

Start date: January 1, 2023
Phase: N/A
Study type: Interventional

The purpose of this research is to explore the effects of chronic androgen exposure on sympathetic nervous system activity (SNSA) and baroreflex control of blood pressure responses in transgender men (trans men) taking gender affirming hormone therapy (HT). Blood pressure, baroreflex gain, and frequency of sympathetic responses to changes in blood pressure will be assessed in trans men and a control group of cisgender women. To fully understand HT effects on blood pressure regulation in trans men, it is crucial to understand how both SNSA, and the pattern of SNSA, can be influenced by high levels of androgen exposure in the female cardiovascular system, as well as how the two regulatory components may interact.