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Hypertension clinical trials

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NCT ID: NCT00876330 Active, not recruiting - Hypertension Clinical Trials

Improving Antihypertensive and Lipid-Lowering Therapy

CERT2
Start date: May 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the impact of electronic health record clinical decision support and automated telephone outreach on antihypertensive and lipid-lowering therapy in ambulatory care.

NCT ID: NCT00875225 Active, not recruiting - Hypertension Clinical Trials

Using Multimedia Technology for Hypertension Control for Low-Income African Americans

CSI Birmingham
Start date: December 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to test an interactive DVD intervention to encourage patients to stick to their blood pressure medication in order to achieve blood pressure control for African American patients. The intervention will convey health messages through personal patient stories who have dealt with or continue to struggle with high blood pressure. Hypothesis 1: At the end of 9 months a higher proportion of patients randomized to the intervention group will achieve appropriate blood pressure control. Hypothesis 2: At the end of 9 months a higher proportion of patients who randomized to the intervention group will report high adherence to their hypertension medications.

NCT ID: NCT00852787 Active, not recruiting - Hypertension Clinical Trials

Marinobufagenin as a Target for DIGIBIND in Hypertensive Patients With End-stage Renal Disease

Start date: April 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study is to examine the effects of the digibind drug on hemodialysis patients with high blood pressure. Digibind is used to treat toxicity from digoxin and digoxin-like molecules which may contribute to high blood pressure.

NCT ID: NCT00742066 Active, not recruiting - Hypertension Clinical Trials

Role of AT1-receptor Blockers in Insulin-induced Vasodilation.

Start date: March 2008
Phase: N/A
Study type: Interventional

In this study we hypothesize that blocking the angiotensin II AT1-receptor improves the insulin-induced microvascular dilatation. Objectives: 1. Does blockade of the angiotensin II AT1-receptor improve the insulin-induced microvascular effects in hypertensive patients. 2. Does blockade of the angiotensin II AT1-receptor impair the insulin-induced microvascular effects in normotensive control subjects?

NCT ID: NCT00694850 Active, not recruiting - Clinical trials for Hypertension, Pulmonary

Impact of Multiple Doses of BAY63-2521 on Safety, Tolerability, Pharmacokinetics and Pharmacodynamics in Patients With Interstitial Lung Disease (ILD) Associated Pulmonary Hypertension (PH)

Start date: August 2, 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess multiple ascending doses of a new drug (BAY63-2521) given orally, to evaluate if it is safe and can help to improve the well-being, symptoms (e.g. disturbed breathing) and outcome of pulmonary hypertension associated with lung fibrosis. Patients living with pulmonary hypertension associated with interstitial lung disease have a risk of increased number of hospitalisations because of worsening of their condition. Until now there is no approved medication for this disease. The current treatment of pulmonary hypertension associated with interstitial lung disease consists: of oxygen and medical treatment with vasodilators, e.g. so-called Calcium-antagonists. Therefore, there is a need for new drugs in the treatment of pulmonary hypertension associated with interstitial lung disease.

NCT ID: NCT00644267 Active, not recruiting - Hypertension Clinical Trials

Using a Telemedicine System to Promote Patient Care Among Underserved Individuals

AHRQ
Start date: April 2008
Phase: N/A
Study type: Interventional

We have established a Telemedicine System for chronic disease management. Based on a personal health record, we have successfully used this system in diverse populations, in over 600 patients, and in multiple disease states (heart failure, CVD risk reduction, gestational diabetes). In this proposal, we will enhance this Telemedicine system to support patient centered care (PCC) by increasing access, incorporating hypertension treatment guideline, quality measures, automating reminders and feedback for both patients and health care providers. Inner-city, primarily African-American patients (N=252) with uncontrolled hypertension (BP<140/90 mmHg) and who are followed by primary care physicians will be randomized to either a usual care or a telemedicine group (Telemedicine plus usual care). Blood pressure, weight, BMI, blood glucose and lipids, and physical activity will be measured at baseline and at 6 months. We hypothesize that more subjects in the telemedicine group will achieve goal blood pressure than in the control group. This will occur through increases in knowledge, self-management, shared decision-making, and improved doctor-patient interaction. Primary end- point will be the proportion of subjects who achieve goal blood pressure. Secondary end-points will include: Rate of self-monitoring, steps per day, weight, CVD knowledge, number of patients at medication guidelines, and increased satisfaction with practice. Telemedicine utilization will also be determined. We believe that telemedicine can facilitate PCC and reduce blood pressure in a cost effective manner.

NCT ID: NCT00631956 Active, not recruiting - Hypertension Clinical Trials

SAPPHIRe III in Taiwan-Progression Evaluation and Cardiovascular Outcomes of Hypertensive Families

Start date: October 2006
Phase: N/A
Study type: Observational

The purpose of this study is to determine the progression evaluation, cardiovascular outcomes, and genetic determinations of hypertension in Chinese

NCT ID: NCT00627159 Active, not recruiting - Hypertension Clinical Trials

ICA-CHAMP: Indo-Central Asian Cardiovascular Health Assessment and Management Program

ICA-CHAMP
Start date: May 2007
Phase: N/A
Study type: Interventional

Research has shown that the presence of heart disease and stroke is higher in the Indo-Asian population compared to other ethno-cultural groups. This may be due to multiple reasons such as a higher presence of diabetes, high blood pressure, high cholesterol, obesity, and lower levels of physical activity. This program will bring together the Calgary Indo-Central-Asian communities and the Calgary Healthcare community to help reduce the rate of heart disease and stroke through a supportive, culturally-sensitive program that is community-based through the following steps: 1. Increase awareness of heart disease and stroke through education among the Calgary Indo-Central-Asian population. 2. Identify early, the risk factors related to heart disease and stroke through screening programs. 3. Provide appropriate follow-up care to the population at risk for heart disease and stroke.

NCT ID: NCT00626964 Active, not recruiting - Hypertension Clinical Trials

Prevention of Coronary Heart Disease in Morbidly Obese Patients

SphCor
Start date: February 2008
Phase:
Study type: Observational

The changes in risks of developing coronary heart disease in patients with morbid obesity after different weight loss interventions have not been extensively studied. The primary objective of this study is to investigate whether an intensive lifestyle intervention program in a tertiary care clinic (Spesialsykehuset for Rehabilitering) is comparable with a 7-week low-energy-diet followed by bariatric surgery in decreasing the risk of cardiovascular disease in these patients.

NCT ID: NCT00617487 Active, not recruiting - Clinical trials for Pulmonary Arterial Hypertension

Pulmonary Arterial Hypertension in Systemic Sclerosis

Start date: December 2007
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate the role of stress echocardiography, compared to standard echocardiography in the early identification of pulmonary arterial hypertension in systemic sclerosis. To evaluate the role of BNP in this setting.To analyze data recorded with respect to the parameters commonly used for SSc evaluation (eg thorax HRCT, pulmonary function tests + DLCO, nailfold capillaroscopy, etc); these parameters are available starting for 1999.