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Blood Pressure clinical trials

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NCT ID: NCT00609271 Completed - Obesity Clinical Trials

Study of Macronutrients and Heart Disease Risk

MACRO
Start date: January 2008
Phase: N/A
Study type: Interventional

The objective of this trial is to examine the long-term effects of a diet low in carbohydrates, as compared to one low in fat, on cardiovascular disease risk factors, including blood pressure (BP), body weight and composition, serum lipids, plasma glucose, insulin, adipocytokines (adiponectin, leptin, resistin), and C-reactive protein (CRP) among obese adults. The investigators will test the following hypotheses: Hypothesis 1: Compared to a low fat diet, a diet low in carbohydrates will reduce systolic and diastolic BP over 12 months; Hypothesis 2: Compared to a low fat diet, a diet low in carbohydrates will reduce body weight, total percent body fat, and waist circumference over 12 months; Hypothesis 3: Compared to a low fat diet, a diet low in carbohydrates will reduce serum levels of LDL-cholesterol and triglycerides and increase serum levels of HDL-cholesterol over 12 months; Hypothesis 4: Compared to a low fat diet, a diet low in carbohydrates will reduce plasma levels of glucose and insulin levels over 12 months; and Hypothesis 5: Compared to a low fat diet, a diet low in carbohydrates will reduce plasma levels of leptin, resistin, and CRP and increase plasma levels of adiponectin over 12 months.

NCT ID: NCT00520247 Completed - Blood Pressure Clinical Trials

Effect of Enalapril Plus Folic Acid on Blood Pressure and Glycometabolism

Start date: September 2005
Phase: Phase 2
Study type: Interventional

Combinded therapy with folic acid and enalapril may significantly decrease plasma total homocysteine level and had beneficial effect on blood pressure reduction and glycometabolism.

NCT ID: NCT00471263 Completed - Blood Pressure Clinical Trials

The Effects of Milk Proteins on Blood Pressure

Start date: May 7, 2007
Phase: N/A
Study type: Interventional

The primary purpose of the study is to demonstrate a blood pressure lowering effect of CasiGold and CasiMax in subjects with high-normal blood pressure or mild hypertension. The secondary purpose is to collect human safety data after treatment with CasiGold and CasiMax, to gain insight into potential mechanisms by measurement of renin and angiotensin I and II, and to evaluate the genetic determinants of the individual BP lowering response by measurement of specific genetic polymorphisms.

NCT ID: NCT00439816 Completed - Hypertension Clinical Trials

Veteran Preference For Group Visits and Its Effect on Hypertension Outcomes

Start date: February 2005
Phase: N/A
Study type: Interventional

To determine racial/ethnic differences in preference for group visits in veterans with poorly controlled hypertension (State 2 hypertension) and determine the effect of group visits on health outcomes among veterans with poorly controlled hypertension.

NCT ID: NCT00379171 Completed - Obesity Clinical Trials

Milk Types and Fish Oil in 9- to 12-Month-Old Infants

Start date: May 2003
Phase: N/A
Study type: Interventional

The objective of this intervention study is to examine the effect of whole cow's milk versus infant formula as primary milk sources with or without supplements of n-3 LCPUFA for growth, nutritional status, development, risk factors for later diseases and the impact on the intestinal microbiota and inflammation in 9 - 12 months old infants.

NCT ID: NCT00240058 Completed - Blood Pressure Clinical Trials

Pilot Study On The Role Of Nitric Oxide In Alpha 1-Adrenergic Vasoreactivity

Start date: July 2005
Phase: N/A
Study type: Interventional

This is a research project to test two study techniques among healthy adults. The procedures look at how blood flow is controlled by substances in blood vessels.

NCT ID: NCT00143988 Completed - Blood Pressure Clinical Trials

Heart Rate and Blood Pressure Response During Exercise and Sexual Activity in Normotensive and Hypertensive Volunteers

SEXERRCISE
Start date: May 2004
Phase: N/A
Study type: Observational

The purpose of this study is to determine the amount of cardiac work as measured by heart rate and blood pressure during physical exertion compared to sexual activity.