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NCT ID: NCT01634464 Recruiting - Obesity Clinical Trials

Role of Nutrition and Maternal Genetics on the Programming of Development of Fetal Adipose Tissue

PREOBE
Start date: March 2007
Phase: N/A
Study type: Observational

In the PREOBE projects it is aimed to obtain genetic and biochemical biomarkers for the programming of obesity in early stages of life. This can be achieved by studying pregnant women with normal weight, overweight, obesity and gestational diabetes, and by analyzing how these conditions could impact on fetal growth and development; the risk of obesity in the offspring during the first 3 years of life will be also assessed (genetic polymorphisms of the most recognized genes related to obesity; gene expression of placental biomarkers indicators of early programming, polyunsaturated fatty acids, immunological and pro-inflammatory markers, analysis of endogenous and exogenous lipid peroxidation, allergies & neurodevelopmental assessment...). Moreover, the interaction of pathological maternal conditions with confounder factors that could have a role in the proposed outcomes will be also studied (maternal and child dietary intake, medical history and socioeconomic & environmental factors).

NCT ID: NCT01633489 Recruiting - Clinical trials for Lysosomal Acid Lipase Deficiency

Lysosomal Acid Lipase (LAL) Deficiency Registry

ALX-LALD-501
Start date: December 31, 2012
Phase:
Study type: Observational [Patient Registry]

This is an observational, multi-center, international disease registry designed to collect longitudinal data and create a knowledge base that will be utilized to improve the care and treatment of patients with LAL Deficiency. Participation in the Registry by both physicians and patients is voluntary.

NCT ID: NCT01630733 Recruiting - Clinical trials for Non-Small Cell Lung Cancer

A Multinational, Randomized, Open-Label Study of Custirsen In Patients With Advanced or Metastatic (Stage IV) Non-Small Cell Lung Cancer

Start date: September 2012
Phase: Phase 3
Study type: Interventional

The primary objective of the study is to compare overall survival of patients randomized to receiving custirsen in combination with docetaxel (Arm A) with patients randomized to receive docetaxel alone (Arm B).

NCT ID: NCT01628068 Recruiting - Clinical trials for Adverse Reaction to Drugs Affecting the Gastrointestinal System

ELIGIBLE (Efficacy of Left atrIal Appendage Closure After GastroIntestinal BLEeding)

ELIGIBLE
Start date: February 2012
Phase: Phase 3
Study type: Interventional

Patients with atrial fibrillation requiring anticoagulation treatment are at high risk of gastrointestinal bleeding. The investigators propose the percutaneous stop the oral anticoagulation and closure of the left atrial appendage with the Amplatzer ® system in patients receiving anticoagulant therapy for atrial fibrillation without associated valvular heart disease, to reduce significantly the risk of stroke while minimizing the risk of bleeding in a group of patients with high risk for both events. ELIGIBLE trial(Left atrial appendage Efficacy of GastroIntestinal Bleeding after closure) is a prospective, multicentric and randomized (2 to 1) trial, comparing percutaneous closure of atrial appendage left versus standard treatment with oral anticoagulants in patients with history of gastrointestinal bleeding and high embolic risk.

NCT ID: NCT01603914 Recruiting - Clinical trials for Catheter-related Bloodstream Infection

Central Venous Catheter Replacement Strategies in Adult Patients With Major Burn Injury

CARB
Start date: May 2012
Phase: N/A
Study type: Interventional

The aim of this project is to answer the following questions: To determine the incidence of catheter related bacteremia (CRB) with three strategies of central venous catheter exchange in critically ill adult patients with major burn and to determine the regimen that will minimize the risk of bacteremia. To determine the incidence rate of catheter colonization in adult patients with major burns. The scientific knowledge to be acquired through this project is of likely benefit to the care of critically ill patients with burns injury as follows: The intention is to improve the outcomes in critically ill patients by minimizing one of the most frequent causes of infection in the Burn Intensive Care Unit, those from central venous catheters. Decreasing infections will decrease morbidity, decrease length of stay, decrease costs, and decrease mortality.

NCT ID: NCT01602939 Recruiting - Clinical trials for Systemic Mastocytosis

Cladribine Plus Pegylated Interpheron Alfa-2a in Systemic Mastocytosis

Start date: May 2012
Phase: Phase 2/Phase 3
Study type: Interventional

The aim of this study is to evaluate the efficacy in terms of clinical and biological response rates of Cladribine plus Pegylated Interpheron alpha-2a therapy in patients with advanced systemic mastocytosis carrying D816V or other exon 17 KIT mutations.

NCT ID: NCT01597479 Recruiting - Clinical trials for Ambulatory Rizarthrosis Surgery

Efficacy of Peripheral Nerve Blocks in Rizarthrosis Ambulatory Surgery

Start date: June 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determinate if peripherical block of radial and median nerves at the elbow guided by ultrasound, and using local anesthetic with a long-term and low concentration, are effective in the treatment of postoperative severe pain due to a selective sensory block at the surgical site.

NCT ID: NCT01595763 Recruiting - Thrombosis Clinical Trials

Diagnostic Approach of Deep Vein Thrombosis in Primary Care

Start date: November 2011
Phase: N/A
Study type: Observational

To asses the cost-effectiveness of implementing different diagnostic strategies in patients with clinical assessment of suspected deep vein thrombosis (DVT) at first presentation in primary care. To evaluate the utility of using D dimer test to diagnose DVT in primary care. To describe the differential diagnosis and the strength of association between each outcome variable and the clinical prediction guide and the final diagnosis. It is a cross-sectional, multicentric study.

NCT ID: NCT01594788 Recruiting - Cardiac Surgery Clinical Trials

Neutrophil Gelatinase-associated Lipocalin as a New Biomarker to Detect Acute Kidney Injury in Postoperative Cardiac Surgery

Start date: April 2011
Phase: N/A
Study type: Observational

Observational study aimed to test the ability of Neutrophil Gelatinase-associated Lipocalin (NGAL) concentration in blood and urine to predict and diagnose early acute renal failure (ARF) in patients after cardiac surgery with/without Cardiopulmonary bypass (CPB).

NCT ID: NCT01586715 Recruiting - Clinical trials for Extremely Complex Perianal Fistulae

Stem Cells Treatment for Extremely Complex Fistulae (HULPCIR)

Start date: March 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the practicability of the autologous e-ASC (Autologous Stem Cells) for the treatment of extremely complex and treatment resistant perianal fistulae.