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Hypertension clinical trials

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NCT ID: NCT00430794 Terminated - Hypertension Clinical Trials

The Efficacy of Spironolactone in Patients With Resistant Hypertension

Start date: March 2007
Phase: Phase 2
Study type: Interventional

To determine the efficacy of the addition of spironolactone to modern blood pressure lowering treatment regimens in patients with resistant hypertension (whose blood pressure is uncontrolled despite three blood pressure lowering drugs)

NCT ID: NCT00430716 Terminated - Clinical trials for Pulmonary Arterial Hypertension

To Assess The Efficacy and Safety Of Oral Sildenafil in the Treatment of Pulmonary Arterial Hypertension.

Start date: April 8, 2008
Phase: Phase 4
Study type: Interventional

To demonstrate a dose response for 1 mg, 5 mg and 20 mg TID oral sildenafil for the treatment of subjects with PAH.

NCT ID: NCT00430040 Terminated - Hypertension Clinical Trials

Vascular Benefits of Adding CarvedilolCR to Type2 Diabetic Patients on ACEI.

Start date: February 2007
Phase: Phase 4
Study type: Interventional

To determine whether addition of Carvedilol CR to diabetic patients with hypertension who are receiving the ACEi,Lisinopril,will provide added benefits to blood vessels when compared to treatment with Lisinopril alone.It is believed that carvedilol provides added benefits by suppressing free radicals(charged substances that cause damage to the body ) and inflammation.

NCT ID: NCT00424801 Terminated - Hypertension Clinical Trials

Effects of Intensive Long-Term Vasodilation in Hypertensive Patients With Microvascular Angina Pectoris

Start date: January 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if long-term vasodilatory treatment is more effective than the standard treatment in hypertensive patients with microvascular angina pectoris

NCT ID: NCT00414869 Terminated - Portal Hypertension Clinical Trials

Preliminary Efficacy and Tolerability of NCX-1000 After Repeated Oral Doses in Patients With Elevated Portal Pressure

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

Chronic liver diseases are often characterized by portal hypertension, a major complication involving haemodynamic changes due to increased intrahepatic vascular resistance. It has become well established that nitric oxide (NO) plays a crucial role in the haemodynamic abnormalities that develop in chronic portal hypertension. NCX-1000 is a NO-releasing derivative of ursodeoxycholic acid that would compensate for the defective liver NO production in cirrhosis. This study intends to demonstrate the desired therapeutic activity (reduction in portal pressure) in a small number of target patients, to assess the safety and tolerability after repeated oral administrations of NCX-1000, and to get preliminary pharmacokinetic data in this population.

NCT ID: NCT00409526 Terminated - Clinical trials for Pulmonary Hypertension

Inhaled Iloprost for the Treatment of Persistent Pulmonary Hypertension in the Term and Near Term Infants.

Start date: December 2006
Phase: Phase 4
Study type: Interventional

Inhaled Iloprost will be administered to near term infants with Persistent Pulmonary Hypertension of the Newborn in two different doses in order to test safety and efficacy in reducing pulmonary artery pressure.

NCT ID: NCT00389675 Terminated - Hypertension Clinical Trials

DORADO-AC-EX - A Long-Term Safety Extension Study to the Phase 3 DORADOC-AC Study (Protocol DAR-312) of Darusentan in Resistant Hypertension

Darusentan
Start date: May 2007
Phase: Phase 3
Study type: Interventional

This is a double-blind, active-controlled, long-term study of a new experimental drug called darusentan. Darusentan in not currently approved by the United States Food and Drug Administration (FDA), which means that a doctor cannot prescribe this drug. The purpose of this study is to evaluate the long-term safety of darusentan (optimized dose) as compared to an active control, administered orally.

NCT ID: NCT00389519 Terminated - Hypertension Clinical Trials

A Study of the Effectiveness and Safety of Ramipril in the Treatment of Hypertension in Children and Adolescents

Start date: October 2006
Phase: Phase 3
Study type: Interventional

The primary purpose of this study is to evaluate the blood pressure lowering effects of ramipril, an FDA-approved drug for the treatment of hypertension in adults, in children and adolescents aged 6 to 16 years with hypertension.

NCT ID: NCT00384865 Terminated - Clinical trials for Hypertension, Pulmonary

A Study of Aspirin and Simvastatin in Pulmonary Arterial Hypertension

Start date: September 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether aspirin and simvastatin are safe and effective for the treatment of pulmonary arterial hypertension (PAH).

NCT ID: NCT00377455 Terminated - Clinical trials for Pulmonary Hypertension

Placebo Controlled Trial of Bosentan in Scleroderma Patients

Start date: September 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether the drug Bosentan improves exercise tolerance in scleroderma patients.