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NCT ID: NCT01159106 Recruiting - Clinical trials for Patient/Ventilator Asynchrony

The Use of Neurally Adjusted Ventilatory Assist (NAVA) Versus Pressure Support During Asynchrony in Children

NAVAChildren
Start date: July 2010
Phase: N/A
Study type: Interventional

The aim of the current study is to compare the application neurally adjusted ventilatory assist (NAVA) to optimize pressure support ventilation in 12 pediatric patients.

NCT ID: NCT01157299 Recruiting - Sepsis Clinical Trials

Hemodynamic Evaluation of Preload Responsiveness in Children by Using PiCCO

PreloaDren
Start date: September 2009
Phase: N/A
Study type: Observational

The purpose of this study is - To assess the value of dynamics (SVV, PPV) and static indices (GEDVI, ITBVI, CVP) of preload and its combination with contractility (CI,SV, ventricular power, dP/dtmax, CFI, GEF) and lung water indices (ELWI), as predictors of fluid responsiveness in both spontaneously breathing and mechanically ventilated pediatric patients. - To assess the value of stroke volume and pulse pressure changes from femoral pulse contour analysis (PiCCO2) during passive leg raising as predictor of fluid responsiveness in pediatric patients. - To establish normal and cutoff values of transpulmonary thermodilution (PiCCO2) hemodynamic variables in hemodynamically stables and hemodynamically "normal" patients.

NCT ID: NCT01141829 Recruiting - Oxidative Stress Clinical Trials

NADPH Oxidase Polymorphisms in Obstructive Sleep Apnea Syndrome (OSAS)

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

Obstructive Sleep Apnea (OSA) is associated with increased oxidative stress. The major sources of Reactive Oxygen Species (ROS) in the vasculature are the NADPH oxidases. Several polymorphisms related to NADPH oxidase expression or NADPH oxidase activity has been identified. The investigators are going to compare the distribution of the allelic frequencies of A-930G and C242T polymorphisms and their possible relationship with the levels of 8-isoprostanes as a marker of oxidative stress in patients with OSA and in a control group without OSA.

NCT ID: NCT01137903 Recruiting - Diabetic Foot Clinical Trials

Efficacy of Surgical Treatment of Osteomyelitis in Diabetic Foot Ulcers

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

Hypothesis:Surgical treatment of osteomyelitis in diabetic foot is more effective that medical treatment through antibiotherapy and leads wound healing in ulcers complicated with bone infection.Material and Methods: Randomized clinical trials which include two groups of patients (n=88), one receives medical treatment through antibiotherapy during 90 days and the other group receive conservative surgical treatment and antibiotics during 7 days after surgery. It will be studied differences between both groups in healing time, recidives, present and relationship of adverse events and outflow of quality of life related health .

NCT ID: NCT01131598 Recruiting - Clinical trials for Acute Respiratory Distress Syndrome

Acute Lung Injury in Children: Epidemiology and Natural History. PEDIATRIC ALIEN.

ALIEN
Start date: January 2010
Phase: N/A
Study type: Observational

The investigators propose to perform a one-year prospective audit of all Acute lung injury (ALI)and cute respiratory distress syndrome (ARDS) pediatric patients managed in several ICUs in Spain. The investigators intend to collect data from all children (from 1 month to 18 years of age) admitted with or developing ALI/ARDS with the aim to understand the epidemiology and natural history of acute lung injury in the pediatric setting. These ICUs are scattered through the Spain and are representative of the demographic differences across the country.

NCT ID: NCT01122758 Recruiting - COPD Clinical Trials

Chronic Obstructive Pulmonary Disease (COPD) History Assessment In SpaiN (CHAIN)

CHAIN
Start date: December 2009
Phase: N/A
Study type: Observational

The research project CHAIN (COPD Assessment History in Spain): "A Multidimensional Study on the Evolution of Chronic Obstructive Pulmonary Disease (COPD)is a multicentre, observational study conducted in several areas of Spain aimed to better define COPD natural history and its phenotypes

NCT ID: NCT01118039 Recruiting - Bladder Cancer Clinical Trials

Sunitinib Malate in Treating Patients With Locally Recurrent, Locally Advanced, Unresectable, or Metastatic Urinary Tract Cancer

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

RATIONALE: Sunitinib malate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. PURPOSE: This phase II trial is studying the side effects of giving sunitinib malate and to see how well it works in treating patients with locally recurrent, locally advanced, unresectable, or metastatic urinary tract cancer.

NCT ID: NCT01116310 Recruiting - Clinical trials for Postmenopausal Women With Moderate Vasomotor Symptoms

Clinical Trial to Evaluate the Efficacy of FITOGYN Versus Placebo on the Vasomotor Symptomatology Associated With Menopause

TRYSEM
Start date: April 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the efficacy of FITOGYN vs. placebo on the vasomotor symptomatology associated with menopause, to evaluate the symptoms of anxiety, the metabolic parameters in menopause and to evaluate the quality of life associated to the vasomotor symptoms of menopause.

NCT ID: NCT01091012 Recruiting - Clinical trials for Pulmonary Hypertension

Effectiveness of the Vasodilator Test With Revatio, Made in Patients With Acute Pulmonary Hypertension

Start date: September 2011
Phase: Phase 3
Study type: Interventional

The main objective is to validate the safety and efficacy of intravenous and oral sildenafil in the acute vasodilator test in patients with persistence of, at least, moderate pulmonary hypertension after valvular surgery successfully, with a correct left ventricular function and no valvular disease hemodynamically significant.

NCT ID: NCT01089842 Recruiting - Atherosclerosis Clinical Trials

Health Coaching to Promote Physical Activity for Coronary Heart Disease Prevention

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

The purpose of this study is to evaluate the efficacy of motivational interviewing-based coaching to increase physical activity to achieve guidelines recommendations for cardiovascular disease prevention.