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Hypertension clinical trials

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NCT ID: NCT00987662 Withdrawn - Obesity Clinical Trials

Irbesartan Versus Amlodipine: The OBI Study

OBI
Start date: January 2012
Phase: Phase 4
Study type: Interventional

Objective: 1. To study the effectiveness of irbesartan 300mg and amlodipine 10 mg in 24h ambulatory blood pressure values in obese subjects 2. To study the drug specific effect in arterial stiffness 3. To study possible drug mechanisms in obesity (reduction of central adiposity and changing the ratio of leptin to adiponectin)

NCT ID: NCT00981591 Withdrawn - Clinical trials for Pulmonary Hypertension

Inhaled Iloprost as an Adjunct to Inhaled Nitric Oxide in Pediatric Critical Care Patients

Start date: September 2009
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine whether inhaled iloprost is safe and effective in pediatric patients with pulmonary hypertension who are sick in the intensive care unit.

NCT ID: NCT00973531 Withdrawn - Hypertension Clinical Trials

Effect of Treating Sleep Disorder Breathing in Patients With Resistant Hypertension

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

The investigators would like to investigate the effects of treating sleep apnea with a positive airway pressure device, either continuous (titrated) versus auto titrated on the control of blood pressure in patients with Resistant Hypertension.

NCT ID: NCT00960921 Withdrawn - Clinical trials for Hypertension, Pulmonary

Study of the Effects of Iron on Lung Blood Pressure at High Altitude

Start date: n/a
Phase: Phase 2
Study type: Interventional

Body iron levels may be important in determining how the blood pressure in the lungs changes in response to low oxygen levels. At high altitude, where oxygen levels are low, some patients develop elevated lung blood pressure. The investigators hypothesize that, in high altitude residents with elevated lung blood pressure, iron supplementation will cause a reduction in lung blood pressure.

NCT ID: NCT00953797 Withdrawn - Hypertension Clinical Trials

Role of Enhanced External Counterpulsation (EECP) Therapy in Patients With Resistant Hypertension

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

High Blood Pressure or Hypertension is one of the main causes of stroke, heart disease, heart attack and kidney disease. Traditionally physicians use diet and lifestyles change and medications to control patient's blood pressure. There are however, some patients whose blood pressures are difficult to control and their blood pressure remains elevated despite multiple medications. When blood pressure remains above goal (greater then 140/90 or greater then 130/80 mmHg in patients with diabetes or kidney disease) despite 3 or more blood pressure medications, the investigators call it "Resistant Hypertension". Enhanced External Counterpulsation (EECP) is a new method of treatment currently used in people with heart disease and chest pain. EECP therapy uses three sets of balloon like cuffs that are wrapped to the calves, lower thighs, and upper thighs. These cuffs inflate and deflate with every heart beat, causing increased blood return to the heart and better blood flow. It has also been found to improve the function of endothelial cells, a type of cells that lines the wall of blood vessel through out the body which helps to regulate and maintain blood pressure. This leads us to believe that EECP therapy, although not used at present for treating patients with Resistant Hypertension, may be useful in decreasing blood pressure.

NCT ID: NCT00922532 Withdrawn - Clinical trials for Hypoxic Respiratory Failure With Pulmonary Hypertension

Inhaled Nitric Oxide (INO) In Hypoxic Respiratory Failure

Start date: November 2009
Phase: Phase 3
Study type: Interventional

This Phase 3, Double-blind, Randomized, Placebo controlled, multicenter study is to confirm the efficacy of inhaled nitric oxide for the management of hypoxic respiratory failure associated with pulmonary hypertension in preterm infants. Study subjects will be administered either inhaled nitric oxide or placebo to determine if there is a change in oxygenation.

NCT ID: NCT00892892 Withdrawn - Hypertension Clinical Trials

Sympathetic Nerve Activity in Renal Failure

SNS in CRF
Start date: November 2009
Phase: Phase 4
Study type: Interventional

The primary purpose is to assess the role of sympathetic activation for the development and progression of chronic renal failure. Using microneurography sympathetic activity will be registered in various stages of kidney affection or failure and hypertension. A sympatholytic agent will be compared with a non-sympatholytic drug to asses the effect sympathetic activation and on the progression of kidney disease. The effects of a sympatholytic agent on cardiovascular reactivity to various stressors wil be examined.

NCT ID: NCT00855517 Withdrawn - Glaucoma Clinical Trials

A Phase 2 Study of the Latanoprost Punctal Plug Delivery System in Subjects With Ocular Hypertension or Open-Angle Glaucoma

Start date: March 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate IOP response to experimental dose of Latanoprost- PPDS in subjects with ocular hypertension or open-angle glaucoma.

NCT ID: NCT00850369 Withdrawn - Sickle Cell Disease Clinical Trials

A Pilot Study of Chronic Red Blood Cell Transfusion in Sickle Cell Disease-Associated Pulmonary Hypertension

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

Pulmonary hypertension, a complication associated with an increased risk of death, is common in patients with sickle cell disease. Despite its frequency, there remains no standard treatment for this complication in patients with sickle cell disease. In this small study, the investigators will evaluate the effect of monthly transfusion of red blood cells to patients with sickle cell disease-associated pulmonary hypertension. The investigators speculate that by increasing the hemoglobin level and decreasing the amount of sickle red blood cells, these patients would experience improvements in their PHT.

NCT ID: NCT00811486 Withdrawn - Clinical trials for Pulmonary Hypertension

Body Volume Regulation in Pulmonary Arterial Hypertension With Right Ventricular Failure

Start date: January 2009
Phase: N/A
Study type: Interventional

Secondary hyperaldosteronism and the non-osmotic release of arginine vasopressin (AVP) are the major factors in sodium and water retention in pulmonary arterial hypertension with right ventricular failure. Natriuretic doses of mineralocorticoid antagonist and aquaretic doses of V2 receptor antagonist will attenuate the sodium and water retention respectively, and be associated with clinical improvement.