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Blood Pressure clinical trials

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NCT ID: NCT01401621 Completed - Clinical trials for Cholesterol Test (Lipid Disorder Screening)

The Effect of a Scratch Off Prompt on Health Engagement

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

The goal of this project is to determine whether prompting the recipient of a health reminder mailing to scratch off targeted area.

NCT ID: NCT01383889 Completed - Blood Pressure Clinical Trials

Acute Maternal and Fetal Effects of Exercise in Pregnancy

EXPREG
Start date: December 2011
Phase: N/A
Study type: Interventional

This will be an open randomized clinical trial involving pregnant women between 35 and 37 weeks randomized to two modalities of exercise: treadmill or stationary bike. The study hypothesis is that exercise on a stationary cycle causes less maternal and fetal effects in relation to treadmill exercise.We will study the acute effects of exercise for both the mother and the fetus, monitoring the parameters before, during and after exercise for 20 minutes. The exercise intensity will be moderate, remaining between 60% and 80% of maximum heart rate. Women will be monitored with a recording equipment of ABPM (ambulatory blood pressure monitorization) and continuous cardiotocography and blood will be collected to measure blood glucose, total cholesterol and HDL, nitrate and lactate before, during and after exercise. The analysis variables are: maternal heart rate and blood pressure, fetal heart rate, number of fetal movements, transient accelerations, decelerations, short-term variability, episodes of high variability, uterine tone, glucose, lactate, nitrate, total cholesterol and HDL.The analysis will be based on intention to treat, according to the recommendations of the CONSORT (2010).

NCT ID: NCT01359748 Completed - Blood Pressure Clinical Trials

Clinical Study About Blood Pressure Measurement Efficacy on Multifunction KEITO

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

The purpose of this trial is to determine the accuracy of the Blood Pressure (BP) measurement of multifunction KEITO devices under test requirements of the Standard American National Standards Institute(ANSI)/Association for the Advancement of Medical Instrumentation(AAMI)/International Organization for Standardization (ISO): ANSI/AAMI/ISO 81060-2:2009.

NCT ID: NCT01357226 Completed - Blood Pressure Clinical Trials

Using the Blood Pressure TRU in Clinical Settings: a Knowledge Translation Study

Start date: May 2011
Phase: N/A
Study type: Observational

Context: Use of automated blood pressure (BP) measurement devices in the office setting is increasingly recognized as superior to manual BP measurement. Current recommendations are to have the patient alone in a quiet room, with no interactions with health care professionals during the readings. However, this may not be practical in primary care offices where the exam rooms are constantly being used. Objective: To compare measurements with an automated BP device in private examination rooms with measurements in non-private areas of a primary care office. Design: Randomized controlled trial with cross-over. Setting: Community based primary care office participating in the NorTReN Practice Based Research Network in Toronto, Ontario. Participants: Fifty consecutive consenting patients over the age of 18 having their BP checked as part of their routine care. Intervention: Patients will be randomly allocated to either automated BP measurement in an exam room, or in a non-private area of the clinic. After being tested in the first location they will subsequently be tested in the second location with the same device. Main outcome measure: The primary outcome measure is a comparison between the mean systolic values of the automated BP measurements in the two office areas. The investigators will use the t-test for paired samples. The secondary outcome is a comparison of systolic values for patients with previously documented hypertension. The investigators define a clinically meaningful result as a difference of 5 mmHg or more in systolic BP. Conclusion: New technology is more readily adopted if barriers to use are minimized. If the investigators find no differences in BP readings between office locations, physicians will then have the convenience of an additional office area to implement the automated BP measurement device.

NCT ID: NCT01320722 Completed - Obesity Clinical Trials

Study of Vitamin D and Uric Acid Lowering on Kidney and Blood Vessel Function

MODERATE
Start date: March 2011
Phase: N/A
Study type: Interventional

The investigators hypothesize that, among non-hypertensive overweight and obese individuals, treatment of vitamin D deficiency and lowering uric acid concentrations (by either xanthine oxidase inhibition or increased renal excretion) will attenuate renin angiotensin system (RAS) activation, improve endothelial function, and lower blood pressure.

NCT ID: NCT01277614 Completed - Diabetes Clinical Trials

Therapeutic Lifestyle Modifications to Reduce Burden of Chronic Disease

Start date: September 2010
Phase: N/A
Study type: Interventional

The investigators previously established that there was a high burden of disease among all categories of staff at the University of the West Indies, St. Augustine and in many ways, this group is typical of the working class of the Caribbean population. Many had poor lifestyle behaviors, 23.8% had Metabolic Syndrome (MS) with many having one or more MS components. Since most time is spent at work, the workplace is understandably the most logical location to address issues pertaining to health, disease prevention and wellness and on-site programs have yielded many health and other benefits to employees and employers alike. Onwards of the 1980s, numerous studies have been done on work-site intervention programs and these have shown that if a company is able to identify employees at risk for developing health problems and then intervene, health risks and the resulting medical problems are reduced. Such a program, if tailored to meet the needs of participants, may yield similar benefits among the staff of the University of the West Indies.

NCT ID: NCT01267227 Completed - Blood Pressure Clinical Trials

Effect of Pterostilbene on Cholesterol, Blood Pressure and Oxidative Stress

Start date: December 2010
Phase: Phase 2/Phase 3
Study type: Interventional

Pterostilbene is one of several stilbenes found in certain berries, particularly blueberries, that have demonstrated pre-clinical benefit to cholesterol, blood pressure, and oxidative stress. The purpose of this study is to evaluate whether pterostilbene will help control cholesterol and blood pressure, as well as improve markers for oxidative stress in patients with dyslipidemia meeting inclusion criteria. The investigators also want to look at the safety of pterostilbene in these patients.

NCT ID: NCT01219413 Completed - Clinical trials for Chronic Kidney Disease

Influence of Aliskiren on Proteinuria

ALIPRES
Start date: March 2009
Phase: Phase 4
Study type: Interventional

To evaluate the proteinuria lowering efficacy as well as tolerability and safety of the renin inhibitor aliskiren compared with that of placebo and angiotensin converting enzyme inhibitor perindopril in patients with non-diabetic chronic renal disease.

NCT ID: NCT01206959 Completed - Blood Pressure Clinical Trials

Clinical Test for Armed-used Blood Pressure Monitor With Preformed Cuff(Monitor When Being Inflated)

Start date: n/a
Phase: N/A
Study type: Observational

The purpose of this study is to monitor the blood pressure level of the patient using a blood pressure monitor which test the blood pressure level in inflating state . The cuff range in the study is 22cm-48cm

NCT ID: NCT01196806 Completed - Blood Pressure Clinical Trials

Comparison of Measurement of Arterial Blood Pressure by L&T NIBP Module With Invasive Arterial Blood Pressure in Neonates

Start date: n/a
Phase: N/A
Study type: Observational

The purpose of this study is to compare Measurements of Arterial Blood Pressure by L&T NIBP Module With Invasive Arterial Blood Pressure in Neonates.