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Prehypertension clinical trials

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NCT ID: NCT01595516 Completed - Hypertension Clinical Trials

Nebivolol and Endothelial Regulation of Fibrinolysis (NERF)

Start date: February 2012
Phase: Phase 4
Study type: Interventional

The investigators hypothesize that nebivolol will improve endothelial t-PA release in adult humans with elevated blood pressure to a greater extent than either metoprolol or placebo. The investigators further hypothesize that the improvement in the capacity of the vascular endothelium to release t-PA with nebivolol is mediated, in part, by the compound's antioxidant properties.

NCT ID: NCT01587183 Completed - Prehypertension Clinical Trials

Running Against Prehypertension Trial (RAPT): A Pilot Trial

RAPT
Start date: March 2012
Phase: N/A
Study type: Interventional

This study will test strategies to help people with prehypertension adopt a running program to reduce their blood pressure in the long term. This study will be a 12 week intervention of about 40 participants randomized to running educational material, group based running instruction, or group based running instruction focused on form and all given the option to use the supplemental mHealth intervention. The purpose of this study is to collect feasibility, acceptability and preliminary efficacy data in preparation for a larger planned NIH-R01 study.

NCT ID: NCT01577030 Completed - Prehypertension Clinical Trials

Hypotensive Effects of Conventional Dairy Products: Role of Arterial Stiffness

Start date: January 2012
Phase: N/A
Study type: Interventional

Elevated systolic blood pressure is by far the largest single contributor to cardiovascular risks in middle-aged and older adults. Lifestyle modifications, including dietary modifications, are the first line approach for treating and preventing hypertension. The general aim of the proposed study is to address the efficacy of conventional dairy products as part of the normal routine diet for lowing arterial blood pressure in middle-aged and older adults with elevated blood pressure. The investigators hypothesize that the dietary intervention including dairy products will induce significant decreases in arterial blood pressure in this population. A secondary aim will be to test the hypothesis that these reductions in systolic blood pressure will be associated with increases in arterial stiffness/compliance and endothelial vasodilatory function.

NCT ID: NCT01568983 Completed - Hypertension Clinical Trials

The Effects of Polyphenol-rich Berry Juice on Blood Pressure in Hypertensive Subjects

Start date: December 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study is to investigate the effects of berry juices containing different levels of polyphenols on blood pressure and other cardiovascular risk factors. The study is a 12 week double blinded randomized controlled intervention trial. The subjects will be divided in three groups where one receives a placebo juice while the two other will consume 0.5 liter of juice containing different levels of polyphenols. Blood pressure will be monitored and blood samples will be taken.

NCT ID: NCT01483430 Recruiting - Prehypertension Clinical Trials

Effect of Ginseol Kg1 on Blood Pressure Lowering

Start date: September 2011
Phase: Phase 3
Study type: Interventional

In this study, we investigate the effects of Ginseol Kg1 (Korea red ginseng extract) on blood pressure in prehypertensive or stage I hypertensive patients.

NCT ID: NCT01472692 Completed - Hypertension Clinical Trials

Study of Febuxostat Effect on Blood Pressure in Patients With High Normal Blood Pressure

Start date: October 2011
Phase: Phase 4
Study type: Interventional

High normal blood pressure, also called prehypertension, is a significant problem. High uric acid in the blood, the same thing that causes gout, may cause higher blood pressures. The investigators plan to monitor the effects of the drug febuxostat(trade name Uloric) on blood pressure and stiffness of the main blood vessels and see if lowering uric acid has any effect.

NCT ID: NCT01458496 Completed - Prediabetes Clinical Trials

Health Coaching to Effect Lifestyle Behaviour Change

HC
Start date: October 2011
Phase: N/A
Study type: Interventional

A health coaching intervention in those with pre-disease (pre-hypertension or pre-diabetes) but without pre-existing cardiovascular disease will effectively help participants change their lifestyle behaviour and prevent or delay onset of cardiovascular disease.

NCT ID: NCT01434953 Terminated - Prehypertension Clinical Trials

Prehypertension Labeling

Tanya K23
Start date: July 13, 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to find out whether labeling adults with prehypertension has negative effects on clinic blood pressure and quality of life 3 months after diagnosis.

NCT ID: NCT01425424 Terminated - Prediabetes Clinical Trials

Prediabetes, Prehypertension and Vitamin D Supplementation - A Practice Based Clinical Intervention Pilot Study

Start date: April 2012
Phase: N/A
Study type: Interventional

This randomized, double-blind, placebo-controlled, multi-site study is to reverse modest elevations of fasting blood sugar (prediabetes) and resting blood pressure(Prehypertension) or both co existing prediabetes and prehypertension by increasing blood levels of vitamin D. This may reduce the chances of developing diabetes or high blood pressure or both later in life.

NCT ID: NCT01412346 Completed - Hypertension Clinical Trials

Health Effects of a Nordic Diet Rich in Plant-based Foods and Fish

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

The purpose of this study is to investigate the effects of a Nordic diet rich in plant-based foods and fish on indicators of cardiovascular disease risk at two different levels of salt intake. The study is a 20-wk randomized controlled crossover trial. The subjects follow a salt-restricted diet during the study. The study begins with a 4-wk run-in phase for all subjects. After that the subjects are randomly allocated to one of two groups. Group 1 consumes a healthy Nordic low-salt diet enriched with plant-based foods and fish for 16 weeks. Group 2 consumes a low-salt diet for 16 weeks. During the 16 weeks, both groups receive salt and placebo capsules in a double-blind, crossover fashion (8+8 weeks).