Clinical Trials Logo

Hypertension clinical trials

View clinical trials related to Hypertension.

Filter by:

NCT ID: NCT02238444 Recruiting - Hypertension Clinical Trials

Warfarin Prevents Portal Vein Thrombosis in Liver Cirrhotic Patients With Hypersplenism After Laparoscopic Splenectomy

ESWA
Start date: September 1, 2014
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether Warfarin Anticoagulation are effective and safe in Prevention of Portal Vein Thrombosis in Liver Cirrhotic Patients with Hypersplenism after Laparoscopic Splenectomy.

NCT ID: NCT02235519 Recruiting - Obesity Clinical Trials

Pleiotropic Effects of Azilsartan Medoxomil Over Insulin Resistance in Obese, Diabetic and Hypertensive Patients

Start date: January 2014
Phase: Phase 2/Phase 3
Study type: Interventional

The goal of this study is to build a mathematical model to explain the effect of two doses of azilsartan (40 and 80 mg) upon metabolic (insulin resistance, glucose) and inflammatory parameters (cytokines) in function of "metabolic strata" like obesity, type 2 diabetes mellitus, hypertension and their combinations.

NCT ID: NCT02222077 Recruiting - Healthy Clinical Trials

Central Blood Pressure in Adolescents and Young Adults

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

This study aims to investigate in adolescents and young adults: - the 24h diurnal variation of ambulatory central blood pressure - the association of central compared to peripheral blood pressure with indices of asymptomatic target-organ damage

NCT ID: NCT02211365 Recruiting - Clinical trials for Hypertension; Heart Disease, Hypertensive

Registro Campania Salute Network on Hypertension

RCSN
Start date: February 2014
Phase:
Study type: Observational [Patient Registry]

The Registro Campania Salute Network (RCSN) is a prospective registry aimed at improving the management of essential hypertension by integrating the activity of general practitioners (GPs) with that of the hypertension specialist. It involves selected GPs homogeneously allocated in the regional area, and the Hypertension Clinic of the Federico II University in Naples, which served as co-ordinating centre. Through the RCSN system it is possible to store clinical data detected at each visit between the peripheral units and the co-ordinating centre and to support scientific analysis of the dataset.

NCT ID: NCT02210923 Recruiting - Clinical trials for Hypertension Resistant To Conventional Therapy

Effect Baroreflex Activation Therapy on the Carotid Body

Start date: October 2013
Phase: N/A
Study type: Observational

Carotid baroreflex activation therapy (BAT) by the Rheos® system produces a sustained fall in blood pressure in patients with resistant hypertension. Since the activation electrodes are implanted at the level of the carotid sinus, it is conceivable that the nearby located carotid body chemoreceptors are stimulated as well. Physiological stimulation of carotid chemoreceptors not only raises respiration, but it also increases sympathetic activity which may in part counteract the effects of BAT. The aim of the present study is to investigate whether there is evidence for concomitant carotid chemoreflex activation during BAT. We hypothesized that there is no clinically relevant co-activation of the carotid body chemoreceptors during BAT in patients with resistant hypertension.

NCT ID: NCT02207868 Recruiting - Clinical trials for Pulmonary Arterial Hypertension

3D Echo Evaluation of the Ventricles in Sclero Associated Severe PAH

EVA3D
Start date: June 2014
Phase:
Study type: Observational

The aim of the study is to document the left and right ventricular function in patients with sclerodermia associated pulmonal arterial hypertension via 3D echocardiography. The results of this study should help to generate hypothesis for further future studies. The primary hypothesis is that the increased use of modern image guided methods could provide essential aspects for the follow up.

NCT ID: NCT02206165 Recruiting - Clinical trials for Essential Hypertension

A Dose Selection Trial of CKD-330 in Patients With Essential Hypertension

Start date: March 2014
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of Candesartan/Amlodipine combined or alone and select better dose of CKD-330 in essential hypertension patients.

NCT ID: NCT02198456 Recruiting - Clinical trials for Pulmonary Arterial Hypertension WHO Group I

Imaging Control Study, 3D Echo, MR and RHC.

PARIS
Start date: July 2014
Phase:
Study type: Observational

The aim of the study is to intensify the follow up of patients with pulmonary arterial hypertension via modern imaging guided methods in due consideration of the possibilities of three-dimensional echocardiography in order to optimize their specific therapy. The hypothesis is that the increased use of modern imaging guided tools is essential for the follow up.

NCT ID: NCT02178319 Recruiting - Liver Cirrhosis Clinical Trials

Laparoscopic Versus Open Devascularization for Portal Hypertension, a Randomized Controlled Trial

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

Many patients with portal hypertension require surgical treatment each year,and Hassab's operation, or esophagogastric devascularization and splenectomy, is an elective procedure. In recent years,laparoscopic esophagogastric devascularization and splenectomy has been used to treat portal hypertension. However, the potential benefits remain to be demonstrated in the context of a randomized trial. In this study, 120 patients will randomize equally receiving laparoscopic or open esophagogastric devascularization and splenectomy. Inclusion criteria included: platelet count < 50×109/ml, esophageal and gastric varices revealed, agreeing the informed consent. PerioperativeOutcomes are: technical success, blood loose and infusion during the operation, recurrent varicose veins on gastroscopy examination, patterns of reflux on duplex ultrasound examination, complications, platelet and liver function variation, length of hospital stay. Follow-up will last 5 years, and gastroscopy and ultrasonic will perform at 3 months, 1 year, 3 years, and 5 years. Further more, this study was proved by the ethical committee of second hospital of Xi'an jiaotong university.

NCT ID: NCT02164526 Recruiting - Clinical trials for Pulmonary Hypertension Due to Left Heart Disease

Registry for Pulmonary Hypertension Due to Left Heart Disease in China

Start date: January 2013
Phase: N/A
Study type: Observational [Patient Registry]

Left heart disease is the main cause of pulmonary hypertension. With the advent of the aging society, chronic heart failure has become a global public health problem. Therefore the prevalence of pulmonary hypertension due to the left heart disease is increasing. However, there is no research on the prevalence of pulmonary hypertension due to the left heart disease in China. Therefore, the aim of the present study was to describe real-world outcome of Chinese patients with pulmonary hypertension due to the left heart disease and identify factors that may predict outcome. Our study will profile the demographics, clinical course, treatments, and outcomes of pulmonary hypertension due to the left heart disease in China.